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HRID 1029231作成日:2026年10月26日

Lithium borohydride → N-(4-(8-(Hydroxymethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-ylamino)phenyl)benzamide

https://huagongshe.com/reaction/1029231

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium borohydrideHCID 4148881—
反応物Methyl 1-(4-benzamidophenylamino)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridine-8-carboxylateHCID 44205292—
溶媒TetrahydrofuranHCID 8028—
生成物N-(4-(8-(Hydroxymethyl)-6-oxo-5,6-dihydrobenzo[c][1,8]naphthyridin-1-ylamino)phenyl)benzamideHCID 5816810331%

反応手順

Lithium borohydride (33 mg, 1.51 mmol) was added to a stirred solution of 267 (100 mg, 0.22 mmol) in THF (10 mL) at 0° C., and stirred for 20 min. at room temperature, then overnight at 45° C. The reaction solution was quenched with MeOH and H2O, acidified with HCl (1 mL, conc.), and stirred for 20 min. The crude product was purified via HP-LC to provide 273 (29 mg, 31% yield) as a solid. LC-MS (M+H=437, obsd.=437).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08735584B2
出典データセットuspto-grants-2014_05
ORD IDord-432894fb771a4c32b94a39ed2c919576
出典メモuspto-grants-2014_05