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Dimethylformamide diethylacetal → ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylate

HRID 47459
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인쇄 미리보기

반응식

HRID 47459 반응식
C([O:3][CH:4]([O:8][CH2:9][CH3:10])N(C)C)C.[CH3:11][C:12]1[N:16]([C:17]2[CH:18]=[N:19][CH:20]=[CH:21][C:22]=2C(O)=O)[N:15]=[N:14][N:13]=1>ClCCl>[CH3:11][C:12]1[N:16]([C:17]2[CH:18]=[N:19][CH:20]=[CH:21][C:22]=2[C:4]([O:8][CH2:9][CH3:10])=[O:3])[N:15]=[N:14][N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70913Dimethylformamide diethylacetalHCID 221726643-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acid

생성물 1

HCID 22172739ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Dimethylformamide diethyl acetal (46 mL) was added to a suspension of 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylic acid (36 g) in dichloromethane (800 mL). The reaction mixture was stirred at ambient temperature overnight then washed six times with water (500 mL), dried over magnesium sulfated, and concentrated under vacuum. The residue was recrystallized from ethyl acetate/hexanes to provide 40 g of ethyl 3-(5-methyl-1H-tetrazol-1-yl)pyridine-4-carboxylate as a solid.

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후처리

  1. washthen washed six times with water (500 mL)
  2. dry with materialdried over magnesium
  3. concentrationconcentrated under vacuum
  4. customThe residue was recrystallized from ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-e2660c48de33439390b2a581508cb241
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06699878B2

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