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1-(1-(Diphenylmethyl)azetidin-3-yl)-4-ethylpiperazine → 1-(Azetidin-3-yl)-4-ethylpiperazine

HRID 707502
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인쇄 미리보기

반응식

HRID 707502 반응식
C1(C(C2C=CC=CC=2)[N:8]2[CH2:11][CH:10]([N:12]3[CH2:17][CH2:16][N:15]([CH2:18][CH3:19])[CH2:14][CH2:13]3)[CH2:9]2)C=CC=CC=1>[OH-].[Pd+2].[OH-].[C].CO>[NH:8]1[CH2:11][CH:10]([N:12]2[CH2:17][CH2:16][N:15]([CH2:18][CH3:19])[CH2:14][CH2:13]2)[CH2:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 1181624801-(1-(Diphenylmethyl)azetidin-3-yl)-4-ethylpiperazine

생성물 1

HCID 627863071-(Azetidin-3-yl)-4-ethylpiperazine

시약·촉매·용매 2

HCID 178502593HCID 178502593, 화합물촉매HCID 887Methanol용매

실험 절차

To a mixed solution of 1-(1-(diphenylmethyl)azetidin-3-yl)-4-ethylpiperazine (12.7 g, 37.9 mmol) described in Production Example 1-3-1 and methanol (50 mL) was added palladium hydroxide-carbon (5.00 g) at room temperature. The resultant mixture was stirred under a hydrogen atmosphere at room temperature and at 0.35 MPa to 0.40 MPa for 10 hours. The reaction mixture was purged with a nitrogen atmosphere and was then filtrated using Celite. A filtrate was concentrated under a reduced pressure to give the title compound in the form of a mixture (12.4 g) with benzylbenzene. The product was used in the subsequent reaction without further purification.

후처리

  1. customThe reaction mixture was purged with a nitrogen atmosphere
  2. filtrationwas then filtrated
  3. concentrationA filtrate was concentrated under a reduced pressure

출처 및 근거

ORD 기록
ord-dcdc62ac47e14ceca93b6d25d75801ee
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174998B2

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