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Methylamine → Tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate

HRID 2403409
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HRID 2403409 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH:13]=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:15][NH2:16].[BH4-].[Na+]>CO>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH2:13][NH:16][CH3:15])=[O:7])([CH3:4])([CH3:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 6329MethylamineHCID 42278151-Boc-2-FormylpyrrolidineHCID 4311764Sodium borohydride

생성물 1

HCID 53346604Tert-butyl 2-((methylamino)methyl)pyrrolidine-1-carboxylate수율 88.8%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a suspension of 2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (2.68 g) in methanol (30 mL) at room temperature was added a solution of methylamine (831 mg) in methanol (3 mL). The reaction mixture was stirred at room temperature for 72 h and then sodium borohydride (760 mg) and molecular sieves were added. After stirring at room temperature for 2 h, the reaction mixture was filtered and the filtrate reduced in vacuo. The residue was redissolved in dichloromethane (30 mL) and washed with saturated sodium bicarbonate solution (30 mL). The combined organics were washed with brine (30 mL), dried (MgSO4) and reduced in vacuo to give 2-methylaminomethyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a pale yellow oil (2.56 g).

후처리

  1. stirringAfter stirring at room temperature for 2 h
  2. filtrationthe reaction mixture was filtered
  3. dissolutionThe residue was redissolved in dichloromethane (30 mL)
  4. washwashed with saturated sodium bicarbonate solution (30 mL)
  5. washThe combined organics were washed with brine (30 mL)
  6. dry with materialdried (MgSO4)

출처 및 근거

ORD 기록
ord-49bf0b221fad4bc8a811fc6ff0269e4c
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802670B2

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