(1S)-2-Chloro-1-methyl-2-oxoethyl acetate → HCID 53721598, 화합물

HRID 379896

반응식

HRID 379896 반응식
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12]([C:14]1[CH:19]=[C:18]([CH3:20])[CH:17]=[CH:16][N:15]=1)=[O:13].[C:21]([O:24][C@@H:25]([CH3:29])[C:26](Cl)=[O:27])(=[O:23])[CH3:22]>>[C:21]([O:24][C@@H:25]([CH3:29])[C:26]([NH:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12]([C:14]1[CH:19]=[C:18]([CH3:20])[CH:17]=[CH:16][N:15]=1)=[O:13])=[O:27])(=[O:23])[CH3:22]

참가 물질

3

반응물 2

HCID 11094804(1S)-2-Chloro-1-methyl-2-oxoethyl acetateHCID 18368098HCID 18368098, 화합물

생성물 1

HCID 53721598HCID 53721598, 화합물

실험 절차

The title compound was prepared according to the procedure described in Example 19 employing 3-amino-6-chloro-2-(4-methylpyridine-2-carbonyl)indole (Example 70) and (S)-(−)-2-acetoxypropionyl chloride. m.p.: 213-214° C.

출처 및 근거

ORD 기록
ord-86d31a9ec1d14e3a82c59d075181c4f9
출처 데이터셋
uspto-grants-2001_10
특허 번호
US06300363B1

연결된 노트

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