Ammonia → ((S)-1-Carbamoyl-2-methoxyethyl)carbamic acid tert-butyl ester

HRID 243012

반응식

HRID 243012 반응식
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:13][O:14][CH3:15])[C:10](O)=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].C[N:17]1CCOCC1.C(OC(Cl)=O)C(C)C.N>C1COCC1>[C:1]([O:5][C:6](=[O:7])[NH:8][C@H:9]([C:10](=[O:11])[NH2:17])[CH2:13][O:14][CH3:15])([CH3:4])([CH3:3])[CH3:2]

참가 물질

6

반응 조건

온도
-15 °C

실험 절차

To a solution of (S)-2-tertbutoxycarbonylamino-3-methoxypropionic acid (1.13 g, 5.2 mmol) in anhydrous THF (20 mL) at −15° C. was added N-methylmorpholine (0.57 mL, 5.2 mmol) and isobutylchloroformate (0.67 mL, 5.2 mmol) under a nitrogen atmosphere. After 2 minutes, 33% aqueous ammonia (0.45 mL, 7.8 mmol) was added and the resulting mixture was stirred at −15° C. for 2 h. The reaction mixture was allowed to warm to RT and was partitioned between EtOAc and a saturated aqueous solution of NaHCO3. The combined organic fractions were washed with aqueous 5% NaHCO3, water, then dried (MgSO4) and concentrated in vacuo. The resulting pink oil was used without further purification (1.03 g, 91%). 1H NMR (CDCl3, 300 MHz): δ 6.42 (1H, br s), 5.48 (2H, br s), 4.25 (1H, br s), 3.83-3.74 (1H, m), 3.52-3.41 (1H, m), 3.40 (3H, s), 1.42 (9H, s).

후처리

  1. temperatureto warm to RT
  2. customwas partitioned between EtOAc
  3. washThe combined organic fractions were washed with aqueous 5% NaHCO3, water
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe resulting pink oil was used without further purification (1.03 g, 91%)

출처 및 근거

ORD 기록
ord-7ca3eaf7db46462cadb527fae1ebf5b3
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08653089B2

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