Hydrochloric Acid → HCID 178525865、化合物

HRID 442156

反応式

HRID 442156 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:11][C:10](=S)[CH2:9][N:8]=[C:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:6]=2[CH:19]=1.[NH2:20][CH2:21][C:22]([OH:24])=[O:23].C(=O)([O-])[O-].[Na+].[Na+].Cl>O.C(O)C>[C:22]([CH2:21][NH:20][C:10]1[CH2:9][N:8]=[C:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:6]2[CH:19]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[N:11]=1)([OH:24])=[O:23]

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 750GlycineHCID 10340Sodium CarbonateHCID 826706Thionordiazepam

生成物 1

HCID 178525865HCID 178525865、化合物収率 77.5%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒2 回

実験手順

A suspension of 3.5 g of 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-2-thione, 5.5 g of glycine, 5.5 g of sodium carbonate, 100 ml of ethanol and 30 ml of water was refluxed with stirring for an hour and the mixture was poured into water. The pH of the solution was adjusted to 4 by addition of 2N hydrochloric acid and was extracted with chloroform. The mixture was filtered and the filtrate was dried over magnesium sulfate and evaporated to dryness. The gummy residue was crystallized by trituration with methanol and the mixture was filtered. The recovered solid was crystallized from ethanol to obtain 3.1 g (77% yield) of 2-carboxymethylamino-7-chloro-5-phenyl-3H-1,4-benzodiazepine melting at 215°-220° C.

後処理

  1. temperaturewas refluxed
  2. extractionwas extracted with chloroform
  3. filtrationThe mixture was filtered
  4. dry with materialthe filtrate was dried over magnesium sulfate
  5. customevaporated to dryness
  6. customThe gummy residue was crystallized by trituration with methanol
  7. filtrationthe mixture was filtered
  8. customThe recovered solid was crystallized from ethanol

出典と根拠

ORDレコード
ord-81a320b18c4c4c4aa09e4fb72f69d2c3
出典データセット
uspto-grants-1977_08
特許番号
US04044142

関連ノート

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