4-Methylmorpholine → Benzyl 2-carbamoylpyrrolidine-1-carboxylate

HRID 1170508

반응식

HRID 1170508 반응식
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[C:16]([OH:18])=O)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[N:20]1CCOCC1.ClC(OCC)=O>C(Cl)Cl.O>[CH2:1]([O:8][C:9]([N:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[C:16](=[O:18])[NH2:20])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

6

반응 조건

온도
0 °C

실험 절차

Pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (30.0 g, 121 mmol) was dissolved in DCM (180 mL). The solution was cooled to 0° C. and N-methyl-morpholine (12.8 g, 127 mmol) was added over a period of 10 mins. The solution was then cooled to −15° C. and the ethyl chloroformate (13.7 g, 126 mmol) in DCM (30 mL) was added dropwise. The solution was then stirred for 2 hours at −25° C. Next, the solution was placed under NH3 (g) while maintaining the temperature below −20° C. The reaction mixture was then stirred for 1 hour while allowing the temperature to return to 0° C. The solution was poured in H2O (120 mL) and the organic layer was partitioned from the aqueous layer. The organic layer was then washed with 1N HCl (2×50 mL), 1N NaHCO3 (2×50 mL), dried over MgSO4 and concentrated under vacuo to afford 27.8 g (88%) of 2-carbamoyl-pyrrolidine-1-carboxylic acid benzyl ester, as a colorless oil.

후처리

  1. temperatureThe solution was then cooled to −15° C.
  2. temperaturewhile maintaining the temperature below −20° C
  3. stirringThe reaction mixture was then stirred for 1 hour
  4. customto return to 0° C
  5. customthe organic layer was partitioned from the aqueous layer
  6. washThe organic layer was then washed with 1N HCl (2×50 mL), 1N NaHCO3 (2×50 mL)
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated under vacuo

출처 및 근거

ORD 기록
ord-f289272eebc446b2ae950940d83e42bc
출처 데이터셋
uspto-grants-2010_11
특허 번호
US07825256B2

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