1,4-Dioxane hydrochloride → 1-(2-Fluoro-3-(trifluoromethyl)benzoyl)piperazine hydrochloride

HRID 1172454ノート

反応式

HRID 1172454 の反応式
[F:1][C:2]1[C:22]([C:23]([F:26])([F:25])[F:24])=[CH:21][CH:20]=[CH:19][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]1)=[O:5].[ClH:27].O1CCOCC1>CO>[ClH:27].[F:1][C:2]1[C:22]([C:23]([F:26])([F:24])[F:25])=[CH:21][CH:20]=[CH:19][C:3]=1[C:4]([N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5]

参加物

4

実験手順

To a mixture of 7.74 g of tert-butyl 4-(2-fluoro-3-(trifluoromethyl)benzoyl)piperazine-1-carboxylate and 10 ml of methanol was added a hydrochloric acid-1,4-dioxane solution (4 M, 20 ml) followed by stirring at room temperature for 4 hours. The reaction mixture was concentrated in vacuo to give the title compound.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo

出典と根拠

ORDレコード
ord-3226fcc81deb4e769210b241a4538192
出典データセット
uspto-grants-2010_11
特許番号
US07834018B2

反応ノート

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