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Trimethyl orthoformate → 2-Chloro-4-(3-dimethoxymethyl-phenyl)-pyrimidine

HRID 14783
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반응식

HRID 14783 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[CH:9]=[C:10]([CH:13]=[CH:14][CH:15]=2)C=O)[CH:5]=[CH:4][N:3]=1.Cl.O1CCOCC1.[CH3:23][O:24][CH:25](OC)[O:26][CH3:27]>>[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[CH:9]=[CH:10][CH:13]=[C:14]([CH:25]([O:26][CH3:27])[O:24][CH3:23])[CH:15]=2)[CH:5]=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 9005Trimethyl orthoformateHCID 204431481,4-Dioxane hydrochlorideHCID 249019653-(2-Chloro-pyrimidin-4-yl)-benzaldehyde

생성물 1

HCID 866032612-Chloro-4-(3-dimethoxymethyl-phenyl)-pyrimidine

실험 절차

Intermediate 1 (3.69 g) was refluxed for two hours in trimethylorthoformate containing 10 mL of 4N HCl/dioxane. The solvent was removed by rotary evaporation to give product, which showed the expected M+H+ of 265 by LC-MS.

후처리

  1. customThe solvent was removed by rotary evaporation
  2. customto give product, which

출처 및 근거

ORD 기록
ord-7533bb8fdece41aa9e7946c5e94b613b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732444B2

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