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Ammonia → N-[4-Chloro-6-(2,3-xylidino)-2-pyrimidinyl]-aminoacetic acid amide

HRID 637936
노트
인쇄 미리보기

반응식

HRID 637936 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]([NH:17][CH2:18][C:19](OCC)=O)[N:3]=1.[NH3:24].[OH2:25]>>[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]([NH:17][C:18](=[O:25])[CH2:19][NH2:24])[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 962WaterHCID 13413749Ethyl 4-chloro-6-(2,3-xylidino)-2-pyrimidinylaminoacetate

생성물 1

HCID 131714453N-[4-Chloro-6-(2,3-xylidino)-2-pyrimidinyl]-aminoacetic acid amide

반응 조건

온도
120 °C

실험 절차

A suspension of ethyl 4-chloro-6-(2,3-xylidino)-2-pyrimidinylaminoacetate (500 mg) in a 10% ammonia ethanolic solution (5 ml) is heated for 20 hours at 120° C. in closed vessel. The mixture is then diluted with water (10 ml) and filtered, yielding 300 mg of the desired amide (I, 3). By the same method the amides of the following acids have been prepared:

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationfiltered

출처 및 근거

ORD 기록
ord-4c68c3eb9f3d4beea344b09462d00a01
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04559345

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