Trichloroacetimidic acid (S)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl ester → Diethyl (1S,2S,3R,4S)-4-{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy}-3-(2-methylphenyl)cyclohexane-1,2-dicarboxylate

HRID 1393328ノート

反応式

HRID 1393328 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@@H:8]1[C@@H:13]([OH:14])[CH2:12][CH2:11][C@H:10]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[C@H:9]1[C:20]([O:22][CH2:23][CH3:24])=[O:21].[F:25][C:26]([F:47])([F:46])[C:27]1[CH:28]=[C:29]([C@@H:37](OC(=N)C(Cl)(Cl)Cl)[CH3:38])[CH:30]=[C:31]([C:33]([F:36])([F:35])[F:34])[CH:32]=1>>[F:25][C:26]([F:46])([F:47])[C:27]1[CH:28]=[C:29]([C@H:37]([O:14][C@H:13]2[CH2:12][CH2:11][C@H:10]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[C@@H:9]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[C@@H:8]2[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[CH3:1])[CH3:38])[CH:30]=[C:31]([C:33]([F:34])([F:35])[F:36])[CH:32]=1

参加物

3

実験手順

The title compound was prepared from the first eluting isomer diethyl(1S,2S,3R,4S)-3-(2-methylphenyl)-4-hydroxycyclohexane-1,2-dicarboxylate (step G) and (1S)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl-2,2,2-trichloroethanimidoate (Example 6, step E) according to the procedure of Example 6, step F. 1H-NMR (CDCl3): δ: 7.65 (1 H, s), 7.15 (2 H, s), 7.08-6.92 (4 H, m), 4.25 (1 H, q, J=6.0 Hz), 4.20-4.10 (2 H, m), 3.85-3.66 (2 H, m), 3.42 (1 H, m), 3.21 (1 H, t), 2.90-2.79 (2 H, m), 2.35 (1 H, m), 2.25 (1 H, m), 2.22 (3 H, s), 1.69-1.56 (2 H, m), 1.30 (3 H, d, J=6.0 Hz), 1.23 (3 H, t, J=7.2 Hz), 0.77 (3 H, t, J=7.2 Hz). Unreacted starting alcohol could be recovered by flushing the column with EtOAc and reused in the above reaction.

後処理

  1. customcould be recovered
  2. customby flushing the column with EtOAc
  3. customreused in the above reaction

出典と根拠

ORDレコード
ord-ccb4e2cec1514eafbb03e8f188c0bd22
出典データセット
uspto-grants-2008_03
特許番号
US07345083B2

反応ノート

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