Sodium Carbonate → HCID 66704854、化合物

HRID 859902ノート

反応式

HRID 859902 の反応式
[CH2:1]([N:8]1[CH2:12][C@H:11]([CH3:13])[C@@H:10]([C:14]([NH:16][CH:17]2[CH2:19][CH2:18]2)=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1>[CH2:1]([N:8]1[CH2:12][C@H:11]([CH3:13])[C@@H:10]([CH2:14][NH:16][CH:17]2[CH2:19][CH2:18]2)[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

実験手順

(3R,4R)-1-Benzyl-N-cyclopropyl-4-methyl-3-pyrrolidinecarboxamide (70.0 g) was dissolved in toluene (700 mL). While this solution was cooled on an ice bath, a borane-dimethyl sulfide complex (90%, 34.3 mL) was added dropwise. The mixture was then stirred for 15 min and was heat-refluxed. After the reaction mixture was cooled to room temperature, a 10% aqueous solution of Na2CO3 (400 mL) was added and the mixture was stirred at 100° C. for 2 hours. The mixture was cooled to room temperature and the toluene layer was separated. The toluene layer was then washed with water (2×250 mL), was dried over anhydrous sodium sulfate, and was concentrated under reduced pressure. The resulting residue was purified by distillation under reduced pressure to obtain (3S,4R)-1-benzyl-3-cyclopropylaminomethyl-4-methylpyrrolidine (62.1 g) as a colorless oil.

後処理

  1. temperatureWhile this solution was cooled on an ice bath
  2. additiona borane-dimethyl sulfide complex (90%, 34.3 mL) was added dropwise
  3. temperaturewas heat-refluxed
  4. stirringthe mixture was stirred at 100° C. for 2 hours
  5. temperatureThe mixture was cooled to room temperature
  6. customthe toluene layer was separated
  7. washThe toluene layer was then washed with water (2×250 mL)
  8. dry with materialwas dried over anhydrous sodium sulfate
  9. concentrationwas concentrated under reduced pressure
  10. distillationThe resulting residue was purified by distillation under reduced pressure

出典と根拠

ORDレコード
ord-443f33a22c4f4d6590889895c3224acb
出典データセット
uspto-grants-2006_12
特許番号
US07153851B2

反応ノート

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