Methylamine → HCID 15629278, 화합물

HRID 1614351노트

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HRID 1614351 반응식
Cl[CH2:2][C@H:3]1[CH2:7][C@H:6](Cl)[CH2:5][N:4]1[S:9]([C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)(=[O:11])=[O:10].[CH3:19][NH2:20]>CO>[C:15]1([CH3:18])[CH:16]=[CH:17][C:12]([S:9]([N:4]2[CH2:5][C@H:6]3[CH2:7][C@@H:3]2[CH2:2][N:20]3[CH3:19])(=[O:11])=[O:10])=[CH:13][CH:14]=1

참가 물질

4

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온도
110 °C

실험 절차

A Parr bottle was charged with 0.5 g (1.29 mmol) of (2R,4S)-2-chloromethyl-4-chloro-1-(4-toluenesulfonyl)pyrrolidine and 6 ml of methanol and the bottle was tared. Methylamine gas was then bubbled through the methanol solution until 0.4 g (12.9 mol) of the gas had dissolved. The bottle was then sealed and heated to 110° C. After heating for 16 hours, the reaction was cooled and the solvent was evaporated at reduced pressure. The residual solids were partitioned between 50 ml of methylene chloride and 40 ml of 10% aqueous NaOH solution. The layers were separated and the organic layer was washed with 40 additional milliliters of 10% aqueous NaOH solution, and then dried over Na2SO4. Evaporation of the solvent under reduced pressure provided 309 mg of the desired product which represents a 90% yield. M.P.=82°-87° C. [α]D =-16.8° (c=1.038, CH3OH).

후처리

  1. dissolutionhad dissolved
  2. customThe bottle was then sealed
  3. temperatureAfter heating for 16 hours
  4. temperaturethe reaction was cooled
  5. customthe solvent was evaporated at reduced pressure
  6. customThe residual solids were partitioned between 50 ml of methylene chloride and 40 ml of 10% aqueous NaOH solution
  7. customThe layers were separated
  8. washthe organic layer was washed with 40 additional milliliters of 10% aqueous NaOH solution
  9. dry with materialdried over Na2SO4
  10. customEvaporation of the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-d36aaa42fbff4cbdbdb07600c0cc02ec
출처 데이터셋
uspto-grants-1993_03
특허 번호
US05196548

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