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Acetic Anhydride → Furo(3,4-b)pyrazine-5,7-dione

HRID 507805
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HRID 507805 반응식
[N:1]1[CH:6]=[CH:5][N:4]=[C:3]([C:7]([OH:9])=O)[C:2]=1[C:10]([OH:12])=[O:11].C(OC(=O)C)(=O)C>>[N:4]1[CH:5]=[CH:6][N:1]=[C:2]2[C:10]([O:12][C:7](=[O:9])[C:3]=12)=[O:11]
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참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 666282,3-Pyrazinedicarboxylic acid

생성물 1

HCID 78482Furo(3,4-b)pyrazine-5,7-dione

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온도
115 °C

실험 절차

In a clean 500 ml R. B. flask charged pyrazine-2,3-dicaroxylic acid (50 gms) and acetic anhydride (162 gms). The reaction mass was heated to 110-120° C. till the completion of reaction to get pyrazine-2,3-dicarboxylic acid anhydride. After completion of the reaction, excess acetic anhydride was distilled out under vacuum and furthermore charged with methylene dichloride (315 ml) and 2-amino-5-chloropyridine (40 gms) in a lot wise manner at room temperature for 30 min. Further, the reaction mixture was stirred for 2 hours at room temperature. The reaction mass was cooled to 5 to 10° C. for one hour, the product was filtered and washed with chilled methylene dichloride. The solid was charged with methylene dichloride (235 ml), triethylamine (40.9 ml) at a temp. of 0-5° C. followed by ethyl chloroformate (28.1 ml). The reaction mass was stirred at 0-5° C. for 1 hr, water (200 ml) was added to the reaction mixture and the mass stirred at room temperature for 1 hr to obtain the solids. The title compound thus separated was isolated by filtration.

출처 및 근거

ORD 기록
ord-772cf84ff08f43d8b9d1780a47aedf91
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07786304B2

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