Sodium Hydroxide → Famotidine sulfamoyl propanamide

HRID 2413346

反応式

HRID 2413346 の反応式
Cl.Cl.[NH:3]([C:7]1[S:8][CH:9]=[C:10]([CH2:12][S:13][C:14](=N)N)[N:11]=1)[C:4]([NH2:6])=[NH:5].[OH-:17].[Na+].[S:19]([NH:23][C:24](=N)[CH:25]=C)(=[O:22])(=[O:21])[NH2:20]>CO>[S:19]([NH:23][C:24](=[O:17])[CH2:25][CH2:14][S:13][CH2:12][C:10]1[N:11]=[C:7]([NH:3][C:4]([NH2:6])=[NH:5])[S:8][CH:9]=1)(=[O:22])(=[O:21])[NH2:20]

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 178458073HCID 178458073、化合物HCID 178478807(2-Carbamimidamido-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride

生成物 1

HCID 178512701Famotidine sulfamoyl propanamide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a solution of S-(2-guanidino-4-thiazolylmethyl)isothiourea dihydrochloride (307 mg, 1.0 mmol) in methanol (5 ml) under a nitrogen atomosphere there was added 1.0 N sodium hydroxide (3 ml, 3.0 mmol). After stirring for 1/2 hour, a solution of N-sulfamyl acrylamidine (169 mg, 1.0 mol) in methanol (3 ml) was added. There was an instantaneous reaction to give product as indicated by TLC. After stirring for several hours, solvents were evaporated and the residue chromatographed on silica gel eluting with 10-15% methanol/chloroform to obtain pure product. When these fractions were combined and evaporated and the residue dissolved in a minimum amount of methanol and diluted with chloroform, the product slowly crystallized, 120 mg, mp 160°. A mixed melting point with authentic product was not depressed.

後処理

  1. customan instantaneous reaction
  2. customto give product
  3. stirringAfter stirring for several hours
  4. customsolvents were evaporated
  5. customthe residue chromatographed on silica gel eluting with 10-15% methanol/chloroform
  6. customto obtain pure product
  7. customevaporated
  8. dissolutionthe residue dissolved in a minimum amount of methanol
  9. additiondiluted with chloroform
  10. customthe product slowly crystallized

出典と根拠

ORDレコード
ord-90f39c37a1bb445a8744ae80ad3f1521
出典データセット
uspto-grants-1985_01
特許番号
US04496737

関連ノート

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