戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1890243作成日:2026年10月25日

4-Chloro-o-anisic acid → (+/-)-4-Fluoro-2-methoxy-N-(4-oxo-2-pyridin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-yl)-benzamide

https://huagongshe.com/reaction/1890243

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-o-anisic acidHCID 93682—
反応物4-Fluoro-2-methoxybenzoic acidHCID 2774545—
反応物(+/-) 9-Amino-2-pyridin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-oneHCID 66846193—
生成物(+/-)-4-Fluoro-2-methoxy-N-(4-oxo-2-pyridin-4-yl-5,6,8,9-tetrahydro-4H-7-oxa-1,4a-diaza-benzocyclohepten-9-yl)-benzamideHCID 44159612—

反応手順

By analogy with the method described in example 1 (step 1.4), using (+/−) 9-amino-2-pyridin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-one and 4-fluoro-2-methoxy benzoic acid in place of (+/−)-9-amino-2-pyrimidin-4-yl-5,6,8,9-tetrahydro-7-oxa-1,4a-diaza-benzocyclohepten-4-one and 4-chloro-2-methoxy-benzoic acid, the compound, 0.068 g (71%), was obtained as a powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08507470B2
出典データセットuspto-grants-2013_08
ORD IDord-7bd987bb57674e3292dae1f2be6e633d
出典メモuspto-grants-2013_08