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HRID 902318作成日:2026年10月26日

Methanol → [(R)-6-fluoro-8-(2-methoxyphenyl)-3,4-dihydro-2H-chromen-2-yl]methanamine

https://huagongshe.com/reaction/902318

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TriphenylphosphineHCID 11776—
反応物(R)-2-azidomethyl-8-(2-methoxyphenyl)-6-fluoro-chromanHCID 86609113—
溶媒WaterHCID 962—
溶媒1,1-DichloropropaneHCID 6573—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium HydroxideHCID 14923—
生成物[(R)-6-fluoro-8-(2-methoxyphenyl)-3,4-dihydro-2H-chromen-2-yl]methanamineHCID 15942471—

反応手順

To a solution of (R)-2-(azidomethyl)-6-fluoro-8-(2-methoxyphenyl)-chroman (210 mg, 0.67 mmol) in tetrahydrofuran (15 mL) and water (0.5 mL) was added triphenylphosphine (0.21 g, 0.80 mmol) and the reaction mixture stirred at room temperature for 24 hours. Chromatography with 0–10% methanol in ethyl methylene chloride plus 1% NH4OH afforded [(R)-6-fluoro-8-(2-methoxyphenyl)-3,4-dihydro-2H-chromen-2-yl]methanamine as a colorless oil. The oil was dissolved in ethyl acetate and made into its hydrochloride salt (0.95 g, 69%) as a white solid using excess ethereal hydrochloric acid, mp 100° C. decomposed; MS (ES) m/z 288.1 ([M+H]+); [α]D25=−34.64° (c=5.7 mg/0.7 mL MeOH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365095B2
出典データセットuspto-grants-2008_04
ORD IDord-8e5b20030d6648e7a7c80d65b2bf6a29
出典メモuspto-grants-2008_04