Benzylamine → HCID 57469090、化合物

HRID 1928442ノート

反応式

HRID 1928442 の反応式
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl.[F:17][C:18]([F:52])([F:51])[C:19]1[CH:24]=[C:23]([C:25]2[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:33])[F:32])=[CH:27][CH:26]=2)[N:22]=[C:21]([C:35]2[CH:40]=[CH:39][N:38]=[C:37]([C:41]3[CH:42]=[C:43]([S:47](Cl)(=[O:49])=[O:48])[CH:44]=[CH:45][CH:46]=3)[CH:36]=2)[N:20]=1>C1COCC1>[CH2:1]([NH:8][S:47]([C:43]1[CH:44]=[CH:45][CH:46]=[C:41]([C:37]2[CH:36]=[C:35]([C:21]3[N:20]=[C:19]([C:18]([F:17])([F:51])[F:52])[CH:24]=[C:23]([C:25]4[CH:30]=[CH:29][C:28]([C:31]([F:34])([F:32])[F:33])=[CH:27][CH:26]=4)[N:22]=3)[CH:40]=[CH:39][N:38]=2)[CH:42]=1)(=[O:48])=[O:49])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

実験手順

To a cooled (ice-water bath) and stirred mixture of benzylamine (0.32 g, 3.0 mmol), triethylamine (0.29 ml, 2.1 mmol) and THF (4 ml) was added drop wise a solution of 3-{4-[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidin-2-yl]-pyridin-2-yl}-benzenesulfonyl chloride hydrochloride (example I.1) (0.58 g, 1.0 mmol) in THF (6 ml). The mixture was allowed to stir at room temperature for 16 h. Purification of the reaction mixture by flash chromatography on silica gel (ethyl acetate/heptane) and crystallization (dichloromethane/MeOH/hexane) yielded the title compound as a white solid (0.49 g, 85%). MS (ISP) 614.8 [(M+H)+]; mp 202.5° C.

後処理

  1. stirringto stir at room temperature for 16 h
  2. customPurification of the reaction mixture by flash chromatography
  3. customon silica gel (ethyl acetate/heptane) and crystallization (dichloromethane/MeOH/hexane)

出典と根拠

ORDレコード
ord-abd14ff780a74d27b9c8da6972ecb10f
出典データセット
uspto-grants-2012_05
特許番号
US08183262B2

反応ノート

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