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Hydrochloric Acid → cis-(6-Methylpiperidin-3-yl)(pyrrolidin-1-yl)methanone hydrochloride

HRID 931325
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HRID 931325 반응식
[ClH:1].[CH3:2][C@H:3]1[CH2:8][CH2:7][C@@H:6]([C:9]([N:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[O:10])[CH2:5][N:4]1C(OC(C)(C)C)=O>CCOCC>[ClH:1].[CH3:2][C@H:3]1[NH:4][CH2:5][C@@H:6]([C:9]([N:11]2[CH2:15][CH2:14][CH2:13][CH2:12]2)=[O:10])[CH2:7][CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 131735166cis-Tert-butyl 2-methyl-5-(pyrrolidine-1-carbonyl)piperidine-1-carboxylate

생성물 1

HCID 89853697cis-(6-Methylpiperidin-3-yl)(pyrrolidin-1-yl)methanone hydrochloride

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A saturated solution of hydrogen chloride in ether (50 mL) was added to a solution of cis-tert-butyl 2-methyl-5-(pyrrolidine-1-carbonyl)piperidine-1-carboxylate (4.0 g, 13.49 mmol) in ether (10 mL) at 0° C. The reaction mixture was stirred at room temperature for 2 h. The excess ethereal hydrogen chloride was evaporated and the residue was concentrated from diethyl ether to afford cis-(6-methylpiperidin-3-yl)(pyrrolidin-1-yl)methanone hydrochloride (3.0 g). The material was used without further purification.

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후처리

  1. customThe excess ethereal hydrogen chloride was evaporated
  2. concentrationthe residue was concentrated from diethyl ether

출처 및 근거

ORD 기록
ord-bb82f4b6b3f1465e8ab343505a7e7d54
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296745B2

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