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Imidazole → HCID 10845857, 화합물

HRID 231794
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HRID 231794 반응식
Cl[C:2]1[N:7]=[C:6]([O:8][CH2:9][CH3:10])[CH:5]=[C:4]([CH3:11])[N:3]=1.[NH:12]1[CH:16]=[CH:15][N:14]=[CH:13]1>O1CCCC1>[CH2:9]([O:8][C:6]1[CH:5]=[C:4]([CH3:11])[N:3]=[C:2]([N:12]2[CH:16]=[CH:15][N:14]=[CH:13]2)[N:7]=1)[CH3:10]
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참가 물질

4

반응물 2

HCID 795ImidazoleHCID 152886712-Chloro-4-ethoxy-6-methylpyrimidine

생성물 1

HCID 10845857HCID 10845857, 화합물수율 50.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In anhydrous tetrahydrofuran, 173 mg of 2-chloro-4-ethoxy-6-methylpyrimidine was substituted with 68 mg of imidazole. The reaction mixture was treated according to the procedure of Example 5 to yield 103 mg of 4-ethoxy-2-(1-imidazolyl)-6-methylpyrimidine, recrystallized from a mixture of n-hexane and ethyl acetate, having a melting point of 115.5°-116° C.

후처리

  1. additionThe reaction mixture was treated

출처 및 근거

ORD 기록
ord-ac4276e7b6eb4ada9ae53823912d360d
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04849424

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