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2-(2,6-Dichloro-4-nitro-phenylsulfanyl)-benzothiazole-5-carbonitrile → 2-(4-Amino-2,6-dichlorophenylsulfanyl)-benzothiazole-5-carbonitrile

HRID 1865538
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HRID 1865538 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[C:4]([Cl:11])[C:3]=1[S:12][C:13]1[S:14][C:15]2[CH:21]=[CH:20][C:19]([C:22]#[N:23])=[CH:18][C:16]=2[N:17]=1.O.O.[Sn](Cl)(Cl)(Cl)Cl>>[NH2:8][C:6]1[CH:7]=[C:2]([Cl:1])[C:3]([S:12][C:13]2[S:14][C:15]3[CH:21]=[CH:20][C:19]([C:22]#[N:23])=[CH:18][C:16]=3[N:17]=2)=[C:4]([Cl:11])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 221487682-(2,6-Dichloro-4-nitro-phenylsulfanyl)-benzothiazole-5-carbonitrileHCID 85782573Tin tetrachloride dihydrate

생성물 1

HCID 221488262-(4-Amino-2,6-dichlorophenylsulfanyl)-benzothiazole-5-carbonitrile수율 80%

실험 절차

The title compound was prepared using the method of example 270, starting with 2-(2,6-dichloro-4-nitro-phenylsulfanyl)-benzothiazole-5-carbonitrile (262) (1.9 g, 4.97 mmol), tin chloride dihydrate (Aldrich, 5.62 g, 24.9 mmol). Compound 274 (1.40 g, 80%) was obtained as a yellowish solid.

후처리

  1. customThe title compound was prepared

출처 및 근거

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
ORD 기록
ord-532afee4680d4422813184b5c1edf740
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07626033B2

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