Trifluoroacetic acid → (3RS,4S)-4-Amino-2-methyl-hexan-3-ol

HRID 1432404

반응식

HRID 1432404 반응식
[CH3:1][CH:2]([CH:4]([OH:28])[C@@H:5]([NH:8]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:6][CH3:7])[CH3:3].FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:8][C@@H:5]([CH2:6][CH3:7])[CH:4]([OH:28])[CH:2]([CH3:3])[CH3:1]

참가 물질

4

실험 절차

To a stirred solution of (3RS,4S)-2-methyl-4-(trityl-amino)-hexan-3-ol (0.36 g, 1 eq, 0.97 mmol) in DCM (20 mL) under an argon atmosphere at room temperature, was added trifluoroacetic acid (5 mL) dropwise, and the solution was stirred at this temperature for 1 h. The solvent was evaporated in vacuo, the residue was precipitated from ether (10 mL) with hexane (90 mL) with string to give a yellow oil. The solvent was decanted from the oil, and the oil was washed with hexane (20 mL) and dried in vacuo to afford the title compound as a light yellow oil; Yield: 0.13 g (100%). (50% de 3R,4S: 50% de 3S,4S), 1H-NMR (d6-DMSO, 250 MHz): δ 0.85-1.01 (m, 9H, NH2CH(CH2CH3)CH(CH(CH3)2)OH), 1.44-1.76 (m, 2H, NH2CH(CH2CH3)CH(CH(CH3)2)OH), 2.94 (m, 1H, NH2CH(CH2CH3)CH(CH(CH3)2)OH), 3.17 (m, 1H, NH2CH(CH2CH3)CH(CH(CH3)2)OH), 3.40 (m, 1H, NH2CH(CH2CH3)CH(CH(CH3)2)OH), 7.54 (bs, 2H, NH2CH(CH2CH3)CH(CH(CH3)2)OH).

후처리

  1. customThe solvent was evaporated in vacuo
  2. customthe residue was precipitated from ether (10 mL) with hexane (90 mL) with string
  3. customto give a yellow oil
  4. customThe solvent was decanted from the oil
  5. washthe oil was washed with hexane (20 mL)
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-81cc2243cbae4a61aeca5490575d70de
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07612079B2

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