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4,6-Dimethoxy-2-(2-nitrobenzyl)pyrimidine → 2-(4,6-Dimethoxypyrimidin-2-ylmethyl)aniline

HRID 743976
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인쇄 미리보기

반응식

HRID 743976 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[N+:18]([O-])=O)[N:4]=1>C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[NH2:18])[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 539772304,6-Dimethoxy-2-(2-nitrobenzyl)pyrimidine

생성물 1

HCID 537780302-(4,6-Dimethoxypyrimidin-2-ylmethyl)aniline수율 83.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The product of stage (i) (32.6 g) was added to a stirred suspension of stannous chloride dihydrate (133 g) in ethanol (300 ml). After refluxing for 2 hours, the solution was poured into ice-water (2500 ml) and extracted with ethyl acetate (3×500 ml). The combined extracts were washed with saturated sodium chloride solution, dried and evaporated to give 24.3 g of the desired product as a brown solid, mp 82°-84° C.

후처리

  1. temperatureAfter refluxing for 2 hours
  2. extractionextracted with ethyl acetate (3×500 ml)
  3. washThe combined extracts were washed with saturated sodium chloride solution
  4. customdried
  5. customevaporated

출처 및 근거

ORD 기록
ord-adf3e20eb4b147c39b65c2b8932dc558
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05559081

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