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Sodium hydride → 1-[3-Chloro-2-(5-methyl-benzothiazol-2-ylsulfanyl)-5-nitro-phenyl]-ethanone

HRID 1865533
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HRID 1865533 반응식
[SH:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:5]=2[N:6]=1.Cl[C:13]1[C:18]([Cl:19])=[CH:17][C:16]([N+:20]([O-:22])=[O:21])=[CH:15][C:14]=1[C:23](=[O:25])[CH3:24].[H-].[Na+]>CN(C=O)C>[Cl:19][C:18]1[C:13]([S:1][C:2]2[S:3][C:4]3[CH:10]=[CH:9][C:8]([CH3:11])=[CH:7][C:5]=3[N:6]=2)=[C:14]([C:23](=[O:25])[CH3:24])[CH:15]=[C:16]([N+:20]([O-:22])=[O:21])[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 221487381-(2,3-Dichloro-5-nitro-phenyl)-ethanoneHCID 178423568HCID 178423568, 화합물

생성물 1

HCID 221487501-[3-Chloro-2-(5-methyl-benzothiazol-2-ylsulfanyl)-5-nitro-phenyl]-ethanone수율 98%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

The title compound was prepared using the method of example 258, starting with 5-methyl-benzothiazole-2-thiol (245) (1.90 g, 10.5 mmol), 1-(2,3-dichloro-5-nitro-phenyl)-ethanone (248) (2.45 g, 10.5 mmol) and NaH (Aldrich, 60% suspension, 420 mg, 10.5 mmol) in DMF (20 mL). Compound 264 (3.87 g, 98%) was obtained as a yellow solid.

후처리

  1. customThe title compound was prepared

출처 및 근거

ORD 기록
ord-2eec59a7d364420ca46e490f8d41e0f6
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07626033B2

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