拉呋替丁

拉呋替丁 基本信息
CAS号 118288-08-7 分子式 C22H29N3O4S
分子量 431.54800 精确质量  431.18800
PSA  103.88000 LogP  3.85510

基本信息 展开↓

CAS号:
118288-08-7
3D弹球模型:
立即前往扯扯看
分子式:
C22H29N3O4S
分子量:
431.54800
中文名称:
拉呋替丁
英文名称:
Lafutidine
中文别名:
拉呋替丁;
(+/-)-2-[(2-呋喃基甲基)亚硫酰]-N-[4-[4-(1-哌啶基甲基)-2-吡啶基]氧-(E)-2-丁烯基]乙酰胺;
(±)-2-[(2-呋喃基甲基)亚硫酰]-N-[4-[4-(1-哌啶基甲基);
(+/-)-2-[(2-呋喃基甲基)亚硫酰]-N-[4-[4-(1-哌啶基甲基)-2-吡啶基]氧-(Z)-2-丁烯基]乙酰胺;
拉夫替丁
英文别名:
Lafutidine;
rac-2-(furfurylsulfinyl)-N-[(Z)-4-{[4-(piperidinomethyl)-2-pyridyl]oxy}but-2-enyl]acetamide;
LAFUTIDINE(SUBJECTTOPATENTFREE);
Protecadin;
(+/-)-2-(furfurylsulfinyl)-N-[4-[4-(piperidinomethyl)-2-pyridyl]oxy-(Z)-2-butenyl]acetamide;
Laflutidine;
enyl)acetamide;
(z)-inyl)oxy)-2-butenyl);
Stogar
精确分子量/精确质量:
431.18800
极性分子表面积/PSA:
103.88000
油水分配系数/LogP:

LogP值指的是某物质在正辛醇/水两相体系中的分配系数的对数值,反映了物质在油水两相中的分配情况。其中、LogP值越大,说明该物质越亲油;反之,LogP值越小,则说明该物质越亲水。
InChI:
InChI=1/C22H29N3O4S/c26-21(18-30(27)17-20-7-6-14-28-20)23-9-2-5-13-29-22-15-19(8-10-24-22)16-25-11-3-1-4-12-25/h2,5-8,10,14-15H,1,3-4,9,11-13,16-18H2,(H,23,26)/b5-2-

生产制备方法及用途展开↓

制备方法


将氢化钠悬浮于四氢呋喃中,在室温滴加(Z)-4-四氢吡喃氧基-2-丁烯醇的四氢呋喃溶液,搅拌,依次加入2-氯-4-哌啶基甲基吡啶和二甲基甲酰胺,反应完毕,经处理得到(Z)-4-哌啶基甲基-2-(4-四氢吡啶氧基-2-丁烯-氧基)吡啶。该化合物溶于甲醇,在冰浴冷却下,加入对甲苯磺酸单水合物,搅拌反应,经处理得到(Z)-4-[4-(哌啶基甲基)吡啶-2-氧基]-2-丁烯醇。该化合物和三乙胺溶于甲苯,在冰浴冷却下滴加甲磺酰氯的甲苯溶液,搅拌,经处理得到溶液。在2-呋喃甲基亚磺酰基乙酰胺的甲苯溶液中加入叔丁氧钾,滴加上面得到的溶液反应,经处理得到拉呋替丁。

合成制备方法


将氢化钠悬浮于四氢呋喃中,在室温滴加(Z)-4-四氢吡喃氧基-2-丁烯醇的四氢呋喃溶液,搅拌,依次加入2-氯-4-哌啶基甲基吡啶和二甲基甲酰胺,反应完毕,经处理得到(Z)-4-哌啶基甲基-2-(4-四氢吡啶氧基-2-丁烯-氧基)吡啶。该化合物溶于甲醇,在冰浴冷却下,加入对甲苯磺酸单水合物,搅拌反应,经处理得到(Z)-4-[4-(哌啶基甲基)吡啶-2-氧基]-2-丁烯醇。该化合物和三乙胺溶于甲苯,在冰浴冷却下滴加甲磺酰氯的甲苯溶
液,搅拌,经处理得到溶液。在2-呋喃甲基亚磺酰基乙酰胺的甲苯溶液中加入叔丁氧钾,滴加上面得到的溶液反应,经处理得到拉呋替丁。

用途简介


拉呋替丁API。

用途


为强效、长效的第二代组胺H2受体拮抗剂,具有独特的胃保护作用。可减少胃酸的基础分泌量,抑制组胺、胃泌素、乌拉坦刺激的胃酸分泌。与西咪替丁、法莫替丁等同类药相比,对H2受体的阻断作用更有效、持久,所以具有抗胃酸分泌作用更加持续的优点。主要用于治疗胃溃疡、十二指肠溃疡和急或慢性胃炎。

物化性质展开↓

密度:
1.252 g/cm3
沸点:
704.2ºC at 760 mmHg
闪点:
379.7ºC
折射率:
1.598
蒸汽压:
1.12E-19mmHg at 25°C
其它信息:

1.性状:类白色或淡黄色结晶性粉末,有异臭,味微苦且涩

2.熔点(ºC):92.7~94.9。

3.溶解性:易溶于DMF、冰乙酸,溶于甲醇,几乎不溶于水。

安全信息展开↓

海关代码:
2929909090
危险类别码:
R36/37/38:Irritating to eyes, respiratory system and skin .
安全说明:
S26-S36/37/39
危险标志:
Xi

合成路线查看所有的合成路线

  • 110-89-4

    哌啶

  • +

  • 118287-95-9

    (Z)-N-(4-((4-formylpyridin-2-yl)oxy)but-2-en-1-yl)-2-((furan-2-ylmethyl)sulfinyl)acetamide

  • 118288-08-7

    拉呋替丁

  • 118289-23-9

    (Z)-N-(4-((4-(1,3-dioxolan-2-yl)pyridin-2-yl)oxy)but-2-en-1-yl)-2-((furan-2-ylmethyl)sulfinyl)acetamide

  • 118288-08-7

    拉呋替丁

  • 118289-21-7

    (Z)-2-(4-((4-(1,3-dioxolan-2-yl)pyridin-2-yl)oxy)but-2-en-1-yl)isoindoline-1,3-dione

  • 118288-08-7

    拉呋替丁

毒理性展开↓

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AC2957000
CHEMICAL NAME :
Acetamide, 2-((2-furanylmethyl)sulfinyl)-N-(4-((4-(1-piperidinyl methyl)-2-pyridinyl)o xy)- 2-butenyl)-, (Z)-
CAS REGISTRY NUMBER :
118288-08-7
LAST UPDATED :
199607
DATA ITEMS CITED :
10
MOLECULAR FORMULA :
C22-H29-N3-O4-S
MOLECULAR WEIGHT :
431.60

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1248 mg/kg
TOXIC EFFECTS :
Behavioral - altered sleep time (including change in righting reflex) Behavioral - convulsions or effect on seizure threshold Gastrointestinal - changes in structure or function of salivary glands
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,143,1995
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
84 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory depression
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,143,1995
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1034 mg/kg
TOXIC EFFECTS :
Behavioral - somnolence (general depressed activity) Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory depression
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,143,1995
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
47900 ug/kg
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - respiratory depression
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,143,1995
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>400 mg/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - convulsions or effect on seizure threshold Gastrointestinal - nausea or vomiting
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,417,1995 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
36400 mg/kg/52W-I
TOXIC EFFECTS :
Liver - changes in liver weight Blood - changes in serum composition (e.g. TP, bilirubin, cholesterol) Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other transferases
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,167,1995
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
9100 mg/kg/13W-I
TOXIC EFFECTS :
Kidney, Ureter, Bladder - proteinuria Kidney, Ureter, Bladder - changes in bladder weight
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,149,1995
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
14 gm/kg/2W-I
TOXIC EFFECTS :
Liver - changes in liver weight Kidney, Ureter, Bladder - changes in bladder weight
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,149,1995
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
9100 mg/kg/13W-I
TOXIC EFFECTS :
Behavioral - convulsions or effect on seizure threshold Blood - other changes Related to Chronic Data - death
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,421,1995
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
10920 mg/kg/52W-I
TOXIC EFFECTS :
Gastrointestinal - hypermotility, diarrhea Blood - changes in serum composition (e.g. TP, bilirubin, cholesterol) Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - transaminases
REFERENCE :
OYYAA2 Oyo Yakuri. Pharmacometrics. (Oyo Yakuri Kenkyukai, CPO Box 180, Sendai 980-91, Japan) V.1- 1967- Volume(issue)/page/year: 50,439,1995

海关数据查看详细

中国海关编码:2929909090

概述:
2929909090 其他含氮基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:30.0%
申报要素:
品名, 成分含量, 用途
摘要/Summary:
2929909090 other compounds with other nitrogen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

分子结构与计算化学数据展开↓

分子结构数据


1、  摩尔折射率:117.69

2、  摩尔体积(cm3/mol):344.6

3、  等张比容(90.2K):958.6

4、  表面张力(dyne/cm):59.8

5、  极化率(10-24cm3):46.65

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