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Di-tert-butyl dicarbonate → HCID 89964768, 화합물

HRID 1846223
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인쇄 미리보기

반응식

HRID 1846223 반응식
Br[C:2]1[C:7]([N:8]([CH2:16][CH2:17][CH:18]=C)[C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:6][CH:5]=[CH:4][N:3]=1.BrC1C(NCCC=C)=CC=CN=1.CC([O:36]C(OC(OC(C)(C)C)=O)=O)(C)C>C(Cl)Cl>[O:36]=[C:18]1[C:2]2[C:7](=[CH:6][CH:5]=[CH:4][N:3]=2)[N:8]([C:9]([O:10][C:11]([CH3:12])([CH3:13])[CH3:14])=[O:15])[CH2:16][CH2:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 90495Di-tert-butyl dicarbonateHCID 89964350HCID 89964350, 화합물HCID 131732430HCID 131732430, 화합물

생성물 1

HCID 89964768HCID 89964768, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

tert-butyl (2-bromopyridin-3-yl)(but-3-en-1-yl)carbamate. To a solution of 2-bromo-N-(but-3-en-1-yl)pyridin-3-amine (1 eq.) and DCM (0.2 M) is added (Boc)2O (1.5 eq.). The solution is stirred at room temperature until judged complete by TLC. The solution is concentrated in vacuo and purified by column chromatography to give the title compound.

후처리

  1. concentrationThe solution is concentrated in vacuo
  2. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-9bbedc54a0a5418694bb09e5e4ee9ab2
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952009B2

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