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Methanol → HCID 14327548, 화합물

HRID 981478
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HRID 981478 반응식
[CH3:1][OH:2].C[O-].[Na+].Cl[C:7]1[CH:12]=[C:11]([CH3:13])[N:10]=[C:9]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=2)[N:8]=1.O>CN(C)C=O>[Cl:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][C:9]2[N:8]=[C:7]([O:2][CH3:1])[CH:12]=[C:11]([CH3:13])[N:10]=2)=[CH:16][CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 962WaterHCID 43459964-chloro-N-(4-chlorophenyl)-6-methylpyrimidin-2-amineHCID 10942334Sodium Methoxide

생성물 1

HCID 14327548HCID 14327548, 화합물수율 88%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
70 °C

실험 절차

A 28% methanol solution of sodium methylate (1.5 g) was added to a solution of 1.5 g of 4-chloro-2-(4-chloroanilino)-6-methylpyrimidine in 50 ml of dimethylformamide and the mixture was stirred for 2 hours at 70° C. After completion of the reaction, the reaction mixture was poured into water, extracted with 150 ml of toluene, washed with water, dried over Glauber's salt, and the toluene layer was concentrated by evaporation. The residue was purified by silica gel column chromatography to obtain 1.3 g (yield: 88%) of 2-(4-chloroanilino)-4-methoxy-6-methylpyrimidine having a melting point of 101°-103° C.

후처리

  1. customAfter completion of the reaction
  2. extractionextracted with 150 ml of toluene
  3. washwashed with water
  4. dry with materialdried over Glauber's salt
  5. concentrationthe toluene layer was concentrated by evaporation
  6. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-4be989f880524bffa43f898f9952bf2a
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04992438

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