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Hydrochloric Acid → HCID 178485080, 화합물

HRID 444003
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HRID 444003 반응식
[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:19][CH3:20])=[N:16][C:17]#[N:18])[N:9]=1)[C:2]([NH2:4])=[NH:3].[ClH:21].C[OH:23]>>[ClH:21].[NH:1]([C:5]1[S:6][CH:7]=[C:8]([CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:19][CH3:20])=[N:16][C:17](=[O:23])[NH2:18])[N:9]=1)[C:2]([NH2:4])=[NH:3]
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참가 물질

4

반응물 3

HCID 313Hydrochloric Acid2회HCID 887MethanolHCID 178485064HCID 178485064, 화합물

생성물 1

HCID 178485080HCID 178485080, 화합물

실험 절차

A mixture of 2-guanidino-4-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]thiazole (1.0 g.), and 2.5 N hydrochloric acid (12 ml.) was heated for four minutes on the steam bath. On cooling a white solid precipitated which was applied to Merck 60 F-254 preparative thin layer chromatography plates and eluted with chloroform/methanol/ammonia (s.g. 0.880) 7:3:0.5 v/v/v. The yellow foam obtained was dissolved in methanol and methanolic hydrogen chloride added. The solution was evaporated to dryness and the residue crystallized from methanol to give 2-guanidino-4-[2-(2-carbamoyl-3-methylguanidino)ethylthiomethyl]thiazole hydrochloride, m.p. 148°-150° C.

후처리

  1. temperaturewas heated for four minutes on the steam bath
  2. temperatureOn cooling a white solid
  3. customprecipitated which
  4. washeluted with chloroform/methanol/ammonia (s.g. 0.880) 7:3:0.5 v/v/v
  5. customThe yellow foam obtained
  6. customThe solution was evaporated to dryness
  7. customthe residue crystallized from methanol

출처 및 근거

ORD 기록
ord-cf9fc630139c43d4a63830ff66f7d018
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04262126

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