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Acetic Acid → HCID 14075369, 화합물

HRID 986595
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HRID 986595 반응식
[C:1]1([C:7]2O[C:9]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:10][C:11](=[O:17])[C:12]=2[C:13]([O:15][CH3:16])=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.CO.[CH3:26][NH2:27].C(O)(=O)C>O>[C:1]1([C:7]2[N:27]([CH3:26])[C:9]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:10][C:11](=[O:17])[C:12]=2[C:13]([O:15][CH3:16])=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 887MethanolHCID 6329MethylamineHCID 14075269HCID 14075269, 화합물

생성물 1

HCID 14075369HCID 14075369, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

3.0 gms of 2,6-diphenyl-3-methoxycarbonyl-pyr-4-one, 33 mls of methanol, 13.3 mls of 40% aqueous methylamine and 2 mls of glacial acetic acid were mixed at room termperature. The next day the mixture was diluted with water. Filtration of the resulting suspension yielded 2.5 gms of methyl 2,6-diphenyl-1-methyl-4-oxonicotinate. Recrystallization from methanol provided material at 255°-7°.

후처리

  1. filtrationFiltration of the resulting suspension

출처 및 근거

ORD 기록
ord-3724c737ca2c4d4fb44d7935a5a85f71
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04714492

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