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Sodium Methoxide → 2(1H)-Pyrimidinimine, 1-[2-(2-bromophenyl)ethyl]-

HRID 1076571
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반응식

HRID 1076571 반응식
C[O-].[Na+].[Br-].[NH2:5][C:6]1[N:11]=[CH:10][CH:9]=[CH:8][N+:7]=1[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[Br:20]>CO>[NH:5]=[C:6]1[N:11]=[CH:10][CH:9]=[CH:8][N:7]1[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[Br:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 12255218HCID 12255218, 화합물

생성물 1

HCID 122552202(1H)-Pyrimidinimine, 1-[2-(2-bromophenyl)ethyl]-수율 81.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3.3 g of sodium methoxide in 120 ml of anhydrous methanol is added 10.8 g of 2-amino-1-(o-bromophenethyl)pyrimidinium bromide, prepared as described in example 1 (G). The solution is stirred under nitrogen for 2 hours and then heated under reflux for 5 hours. The solvent is removed in vacuo and the residue is treated with 200 ml of anhydrous ether. The ether solution is washed, dried, and concentrated in vacuo to give about 6.8 g of yellow solid. This is recrystallized from hexane to give the name product, mp about 97°-98°.

후처리

  1. customprepared
  2. temperatureheated
  3. temperatureunder reflux for 5 hours
  4. customThe solvent is removed in vacuo
  5. additionthe residue is treated with 200 ml of anhydrous ether
  6. washThe ether solution is washed
  7. customdried
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2348518e06264c46885f8a96105fd126
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03957787

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