((1S,2S)-2-((S)-1-phenylethylamino)cyclohexyl)methanol → [(1S,2S)-2-aminocyclohexyl]methanol

HRID 2065943ノート

反応式

HRID 2065943 の反応式
C1([C@@H]([NH:9][C@H:10]2[CH2:15][CH2:14][CH2:13][CH2:12][C@@H:11]2[CH2:16][OH:17])C)C=CC=CC=1>[Pd].CO>[NH2:9][C@H:10]1[CH2:15][CH2:14][CH2:13][CH2:12][C@@H:11]1[CH2:16][OH:17]

参加物

4

反応条件

温度
60 °C

実験手順

5% Palladium on carbon (0.05 g) was added to a solution of (1S,2S)-2-[(S)-1-phenylethyl amino]cyclohexyl)methanol (11, 0.5 g, 0.002 mol) dissolved in methanol (15 mL). The mixture was heated at 60° C. under hydrogen (14.5 psi) atmosphere for NLT 3 h. The mixture was cooled to room temperature, flushed with nitrogen, the catalyst was filtered and washed with fresh methanol (10 mL). The combined filtrate was concentrated under vacuum to afford 0.28 g of ((1S,2S)-2-aminocyclohexyl)methanol (17) in quantitative yield as a white solid. [α]23D 9.1 (c, 0.0107 CHCl3), 1H NMR (CDCl3, 400 MHz): δ 3.61-3.54 (m, 2 H), 2.71 (bs, 3H), 2.45 (dt, 1H, J=10.6, 1.2 Hz), 1.85-1.78 (m, 1H), 1.74-1.65 (m, 1H), 1.62-1.53 (m, 1H), 1.40-1.30 (m, 1H), 1.25-1.06 (m, 3H), 0.91-0.80 (m, 1H), 13C NMR (CDCl3): δ 70.2, 57.4, 45.5, 40.1, 28.6, 25.5, 25.5, For NMR of its enantiomer, ((1R,2R)-2-Aminocyclohexyl)methanol, see reference J. Am. Chem. Soc. 1996, 118, 5502.

後処理

  1. temperatureThe mixture was cooled to room temperature
  2. customflushed with nitrogen
  3. filtrationthe catalyst was filtered
  4. washwashed with fresh methanol (10 mL)
  5. concentrationThe combined filtrate was concentrated under vacuum

出典と根拠

ORDレコード
ord-09c14c361118403895db625493221adc
出典データセット
uspto-grants-2012_10
特許番号
US08288565B2

反応ノート

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