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Ammonium Hydroxide → [4-Chloro-6-(2,3-xylidino)-2-pyrimidinylthio]acetamide

HRID 1578944
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인쇄 미리보기

반응식

HRID 1578944 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:10]=2[CH3:16])[N:5]=[C:4]([S:17][CH2:18][C:19]([O:21]CC)=O)[N:3]=1.[OH-].[NH4+:25]>C(O)C>[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:10]=2[CH3:16])[N:5]=[C:4]([S:17][CH2:18][C:19]([NH2:25])=[O:21])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 9798569HCID 9798569, 화합물

생성물 1

HCID 21557341[4-Chloro-6-(2,3-xylidino)-2-pyrimidinylthio]acetamide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5.0 g of [4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio] acetic acid, ethyl ester was added to 40 ml of concentrated ammonium hydroxide. Ethanol (40 ml) was then added and the reaction mixture was boiled to give a clear solution. This solution then stood at room temperature for three days. The precipitate thus formed was collected and recrystallized from ethanol giving 3.0 g of product, mp. 188°-191°C.

후처리

  1. customto give a clear solution
  2. customThe precipitate thus formed
  3. customwas collected
  4. customrecrystallized from ethanol giving 3.0 g of product, mp. 188°-191°C.

출처 및 근거

ORD 기록
ord-006abab5afd54c0da949ef54c3f0af20
출처 데이터셋
uspto-grants-1976_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03940394

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