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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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benzyl 4-(N,N'-bis{[(2-methyl-2-propanyl)oxy]carbonyl}carbamimidoyl)-1-piperazinecarboxylate → [tert-Butoxycarbonylimino(piperazin-1-yl)methyl]carbamic acid tert-butyl ester

HRID 1053826
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HRID 1053826 반응식
[CH3:1][C:2]([O:5][C:6]([NH:8][C:9]([N:18]1[CH2:23][CH2:22][N:21](C(OCC2C=CC=CC=2)=O)[CH2:20][CH2:19]1)=[N:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])=[O:7])([CH3:4])[CH3:3]>C(O)C.[Pd]>[CH3:17][C:14]([O:13][C:11](=[O:12])[NH:10][C:9](=[N:8][C:6](=[O:7])[O:5][C:2]([CH3:4])([CH3:3])[CH3:1])[N:18]1[CH2:19][CH2:20][NH:21][CH2:22][CH2:23]1)([CH3:15])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 131736303benzyl 4-(N,N'-bis{[(2-methyl-2-propanyl)oxy]carbonyl}carbamimidoyl)-1-piperazinecarboxylate

생성물 1

HCID 68635492[tert-Butoxycarbonylimino(piperazin-1-yl)methyl]carbamic acid tert-butyl ester수율 163.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of the compound prepared in Example 27 (0.045 g, 0.056 mmol) in ethanol (10 mL) was added Pd/C (20% by wt, 0.010 g). The reaction was stirred under an atmosphere of hydrogen (40 psi) at room temperature for 2 h. The reaction mixture was filtered through diatomaceous earth and the filtrate concentrated to afford the title compound (0.03 g, 69%) as a pale green solid.

후처리

  1. filtrationThe reaction mixture was filtered through diatomaceous earth
  2. concentrationthe filtrate concentrated

출처 및 근거

ORD 기록
ord-5325d82b197941b09f79600d4ab6510c
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394250B2

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