(Z)-4-amino-N-hydroxy-1,2,5-oxadiazole-3-carbonimidoyl chloride → HCID 178505103, 화합물

반응식

Cl.[NH2:2][CH2:3][CH2:4][CH2:5][NH:6][S:7]([CH3:10])(=[O:9])=[O:8].[NH2:11][C:12]1[C:13]([C:17](Cl)=[N:18][OH:19])=[N:14][O:15][N:16]=1>>[NH2:11][C:12]1[C:13]([C:17](=[N:18][OH:19])[NH:2][CH2:3][CH2:4][CH2:5][NH:6][S:7]([CH3:10])(=[O:9])=[O:8])=[N:14][O:15][N:16]=1

참가 물질

반응물 2

HCID 4040027(Z)-4-amino-N-hydroxy-1,2,5-oxadiazole-3-carbonimidoyl chloride

HCID 86638005N-(3-aminopropyl)methanesulfonamide hydrochloride

생성물 1

HCID 178505103HCID 178505103, 화합물수율 19%

실험 절차

The desired compound was prepared according to the procedure of Example 17, step C, using N-(3-aminopropyl)methanesulfonamide hydrochloride and 4-amino-N-hydroxy-1,2,5-oxadiazole-3-carboximidoyl chloride [made according to Example 1, steps A through B] as the starting materials in 19% yield.

출처 및 근거

ORD 기록: ord-81f4d4a1f2bf4a1fae7610585b2117e8
출처 데이터셋: uspto-grants-2015_03
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US08993605B2

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