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Methanol → 1,3-Dihydro-1-methyl-3-[4-(5-methyl-1H-imidazol-1-yl)-2-butynyl]-2H-imidazol-2-one

HRID 846654
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인쇄 미리보기

반응식

HRID 846654 반응식
Br[CH2:2][C:3]#[C:4][CH2:5][N:6]1[CH:10]=[CH:9][N:8]([CH3:11])[C:7]1=[O:12].C([N:16]1[CH:20]=[C:19]([CH3:21])[N:18]=[CH:17]1)(=O)C.CO>C(#N)C>[CH3:11][N:8]1[CH:9]=[CH:10][N:6]([CH2:5][C:4]#[C:3][CH2:2][N:18]2[C:19]([CH3:21])=[CH:20][N:16]=[CH:17]2)[C:7]1=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 109534921-Acetyl-4-methylimidazoleHCID 150655461-(4-bromo-2-butynyl)-1,3-dihydro-3-methyl-2H-imidazol-2-one

생성물 1

HCID 150655801,3-Dihydro-1-methyl-3-[4-(5-methyl-1H-imidazol-1-yl)-2-butynyl]-2H-imidazol-2-one수율 79.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
85 °C

실험 절차

A mixture of 1-(4-bromo-2-butynyl)-1,3-dihydro-3-methyl-2H-imidazol-2-one (4.12 g, 0.018 mol) and 1-acetyl-4-methylimidazole (4.47 g, 0.036 mol) in acetonitrile (6 mL) was heated in an oil bath (bath temperature 85° C.) for 1 hr. Methanol (20 mL) was added and, after 1 hr, the solvents were removed and the residue was partitioned between ethyl acetate and 4N NaOH solution. The ethyl acetate was removed and the residual oil was chromatographed on silica gel using methanol:chloroform as eluant to give 3.3 g of product.

후처리

  1. customthe solvents were removed
  2. customthe residue was partitioned between ethyl acetate and 4N NaOH solution
  3. customThe ethyl acetate was removed
  4. customthe residual oil was chromatographed on silica gel

출처 및 근거

ORD 기록
ord-3dfa2bada05a46e387658623f86b5387
출처 데이터셋
uspto-grants-1992_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05137905

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