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3-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one → 3-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidine

HRID 2187794
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HRID 2187794 반응식
[C:1]([CH:4]1[CH2:8][CH2:7][N:6]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)[C:5]1=O)(=O)[NH2:2]>C1COCC1>[NH2:2][CH2:1][CH:4]1[CH2:8][CH2:7][N:6]([CH2:9][C:10]2[CH:11]=[CH:12][C:13]([Cl:16])=[CH:14][CH:15]=2)[CH2:5]1
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참가 물질

3

반응물 1

HCID 184262563-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one

생성물 1

HCID 184262513-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidine수율 66.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
65 °C

실험 절차

To a solution of 3-carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one (1.45 g) in THF (15 mL) was added 1.0 N BH3 in THF (25 mL). The reaction mixture was stirred at 65° C. for 15 h. After cooling to room temperature, the solvent was removed under reduced pressure. Water (30 mL) and conc. HCl (10 mL) were added and the mixture was stirred at 100° C. for 2 h and room temperature for 1 h. 2 N NaOH aqueous solution (100 mL) was added and the mixture was extracted with AcOEt (50 mL×3). The combined organic layers were dried over K2CO3, filtered and concentrated. Column chromatography (SiO2, 15% CH3OH—5% Et3N in CH2Cl2) afforded 3-(aminomethyl)-1-(4-chlorobenzyl)pyrrolidine (860 mg, 19%) as a colorless oil.

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe solvent was removed under reduced pressure
  3. additionWater (30 mL) and conc. HCl (10 mL) were added
  4. stirringthe mixture was stirred at 100° C. for 2 h and room temperature for 1 h
  5. addition2 N NaOH aqueous solution (100 mL) was added
  6. extractionthe mixture was extracted with AcOEt (50 mL×3)
  7. dry with materialThe combined organic layers were dried over K2CO3
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-955fb4d0dc9747289e3a10870e361780
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410566B1

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