Diethyl Oxalate → 8-[2-(Benzyloxymethyl)benzofuran-5-carboxamido]-4-oxo-4H-1-benzopyran-2-carboxylic acid
반응식
C(C1C(O)=C(NC(C2C=CC3OC(COCC4C=CC=CC=4)=CC=3C=2)=O)C=CC=1)(=O)C.C(OCC)(=O)C(OCC)=O.[CH2:42]([O:49][CH2:50][C:51]1[O:52][C:53]2[CH:59]=[CH:58][C:57]([C:60]([NH:62][C:63]3[C:72]4[O:71][C:70]([C:73]([O:75]CC)=[O:74])=[CH:69][C:68](=[O:78])[C:67]=4[CH:66]=[CH:65][CH:64]=3)=[O:61])=[CH:56][C:54]=2[CH:55]=1)[C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1>>[CH2:42]([O:49][CH2:50][C:51]1[O:52][C:53]2[CH:59]=[CH:58][C:57]([C:60]([NH:62][C:63]3[C:72]4[O:71][C:70]([C:73]([OH:75])=[O:74])=[CH:69][C:68](=[O:78])[C:67]=4[CH:66]=[CH:65][CH:64]=3)=[O:61])=[CH:56][C:54]=2[CH:55]=1)[C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1참가 물질
4
반응물 3
생성물 1
실험 절차
Following the process described in example 1 (point A), starting from N-(3-acetyl-2-hydroxyphenyl)-2-(benzyloxymethyl)benzofuran-5-carboxamide and diethyl oxalate, ethyl 8-[2-(benzyloxymethyl)benzofuran-5-carboxamido]-4-oxo-4H-1-benzopyran-2-carboxylate was prepared which was subsequently hydrolysed according to the process described in example 1 (point M) to yield the title compound as a white solid with melting point 215-218° C. (65% global yield).
후처리
- customwas prepared which
출처 및 근거
- ORD 기록
- ord-c80e4b8ab5f840fe8016c9da09487413
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05990142
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