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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 23000218, 화합물 → HCID 23000253, 화합물

HRID 398340
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HRID 398340 반응식
[C:1]([N:4]([C:10]1[N:15]=[CH:14][CH:13]=CN=1)[CH2:5][CH2:6][CH2:7][C:8]#[CH:9])(=[O:3])[CH3:2]>[N+](C1C=CC=CC=1)([O-])=O>[C:1]([N:4]1[C:10]2[C:7](=[C:8]([CH3:9])[CH:13]=[CH:14][N:15]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 23000218HCID 23000218, 화합물

생성물 1

HCID 23000253HCID 23000253, 화합물

시약·촉매·용매 1

HCID 7416Nitrobenzene용매

실험 절차

A solution of 2-(N-acetyl-N-pent-4-ynylamino)pyrimidine (3.49 g, 17.2 mmol) in nitrobenzene (35 mL) was heated under argon at 180° C. for 2 days. The reaction mixture was cooled and loaded directly onto a dry silica get column. The column was first eluted with methylene chloride to wash off the nitrobenzene and then was eluted with ether to give after evaporation in vacuo to give the title compound as a pale yellow solid:

후처리

  1. temperatureThe reaction mixture was cooled
  2. customget column
  3. washThe column was first eluted with methylene chloride
  4. washto wash off the nitrobenzene
  5. washwas eluted with ether
  6. customto give
  7. customafter evaporation in vacuo

출처 및 근거

ORD 기록
ord-4660dcf9e4ad498fa43053eaf3ddf8ee
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06610692B1

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