Triethylamine → 2-Benzyloxycarbamoyl-4-methylpentanoic acid ethyl ester

HRID 1516469노트

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HRID 1516469 반응식
[CH2:1]([O:3][C:4](=[O:13])[CH:5]([CH2:9][CH:10]([CH3:12])[CH3:11])[C:6]([OH:8])=O)[CH3:2].[CH2:14](NO)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C1C=CC2[N:31]([OH:32])N=NC=2C=1.C1CCC(N=C=NC2CCCCC2)CC1.C(N(CC)CC)C>C1COCC1.C(Cl)Cl>[CH2:1]([O:3][C:4](=[O:13])[CH:5]([C:6](=[O:8])[NH:31][O:32][CH2:14][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)[CH2:9][CH:10]([CH3:12])[CH3:11])[CH3:2]

참가 물질

8

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온도
0 °C

실험 절차

Intermediate (3a) (40.3 g, 214 mmol, 1.0 eq) was dissolved into 800 mL DCM and 900 mL THF and the solution was cooled to 0° C. To this was added benzyl hydroxylamine (34.2 g, 214 mmol, 1.0 eq) followed by HOBt (28.9 g, 214 mmol, 1.0 eq). The mixture was stirred for 5 minutes, then DCC (44.1 g, 214 mmol, 1.0 eq) was added, followed by triethylamine (33.4 mL, 240 mmol, 1.1 eq). The mixture was warmed to room temperature and stirred overnight. The solid was filtered and the filtrate was concentrated. The material was redissolved in 1000 mL EtOAc and washed with 500 mL 1N HCl, 600 mL saturated aq. bicarbonate, dried over MgSO4, filtered, and evaporated to yield intermediate (3b) (59.3 g) as a semisolid. MS m/z: [M+H+] calcd for C16H23NO4 294.2; found 294.2.

후처리

  1. temperatureThe mixture was warmed to room temperature
  2. stirringstirred overnight
  3. filtrationThe solid was filtered
  4. concentrationthe filtrate was concentrated
  5. dissolutionThe material was redissolved in 1000 mL EtOAc
  6. washwashed with 500 mL 1N HCl, 600 mL saturated aq. bicarbonate
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. customevaporated

출처 및 근거

ORD 기록
ord-170cf364c65444eea225caf63e948a55
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08227497B2

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