4-Bromo-1,1,1-trifluorobutane → 5-tert-butyl-3-(4,4,4-trifluorobutyl)thiazol-2(3H)-imine hydrobromide

HRID 254654

反応式

HRID 254654 の反応式
[C:1]([C:5]1[S:9][C:8]([NH2:10])=[N:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[Br:11][CH2:12][CH2:13][CH2:14][C:15]([F:18])([F:17])[F:16]>>[BrH:11].[C:1]([C:5]1[S:9][C:8](=[NH:10])[N:7]([CH2:12][CH2:13][CH2:14][C:15]([F:18])([F:17])[F:16])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]

参加物

3

反応条件

温度
85 °C

実験手順

A mixture of the product of Example 74A (0.25 g, 1.6 mmol) and 1-bromo-4,4,4-trifluorobutane (336 mg, 1.8 mmol) was warmed to 85° C. and was stirred for 16 hours. The mixture was cooled to ambient temperature and the title compound (0.35 g, 63% yield) was isolated via filtration. MS (DCI/NH3) m/z 267 (M+H)+.

後処理

  1. temperatureThe mixture was cooled to ambient temperature

出典と根拠

ORDレコード
ord-6bd9a4d7479a43eeabafee4851dea8d0
出典データセット
uspto-grants-2011_01
特許番号
US07875640B2

関連ノート

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