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Dimethylformamide → 3,4-Dimethyl-7-(2-methyl-1,3,4-oxadiazol-5-yl)-methoxycoumarin

HRID 1460984
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인쇄 미리보기

반응식

HRID 1460984 반응식
O[C:2]1[CH:11]=[C:10]2[C:5]([C:6]([CH3:14])=[C:7]([CH3:13])[C:8](=[O:12])[O:9]2)=[CH:4][CH:3]=1.Cl[CH2:16][C:17]1[O:18][C:19](C)=[N:20][N:21]=1.CN(C)[CH:25]=[O:26]>[H-].[Na+]>[CH3:13][C:7]1[C:8](=[O:12])[O:9][C:10]2[C:5]([C:6]=1[CH3:14])=[C:4]([O:26][CH3:25])[CH:3]=[C:2]([C:19]1[O:18][C:17]([CH3:16])=[N:21][N:20]=1)[CH:11]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228Dimethylformamide2회HCID 38266202-(Chloromethyl)-5-methyl-1,3,4-oxadiazoleHCID 54129907-hydroxy-3,4-dimethyl-2H-chromen-2-one

생성물 1

HCID 197514643,4-Dimethyl-7-(2-methyl-1,3,4-oxadiazol-5-yl)-methoxycoumarin

시약·촉매·용매 1

HCID 24758Sodium hydride용매

실험 절차

5.0 g of 7-hydroxy-3,4-dimethylcoumarin in 20 ml of 0.9 g of NaH (80%) in 50 ml of dimethylformamide at room temperature. After 45 minutes, 3.5 g of 2-chloromethyl-5-methyl-1,3,4-oxadiazole, dissolved in 20 ml of dimethylformamide, were added and the mixture was stirred overnight at room temperature. The reaction solution was hydrolyzed with ice water, and the precipitated solid was filtered off under suction and recrystallized from methanol.

후처리

  1. customat room temperature
  2. additionwere added
  3. filtrationthe precipitated solid was filtered off under suction
  4. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-576d4fd965194fd09ab516e8d6164556
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05073563

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