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HRID 715727作成日:2026年10月26日

Triphenylphosphine → 1-[(S)-1-(4-Methoxy-phenyl)-ethyl]-(R)-4-[(R)-1-[7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridin-5-yloxy]-ethyl]-pyrrolidin-2-one

https://huagongshe.com/reaction/715727

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物(R)-4-((S)-1-hydroxyethyl)-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-oneHCID 58071870—
反応物HCID 178487380HCID 178487380—
溶媒TetrahydrofuranHCID 8028—
生成物1-[(S)-1-(4-Methoxy-phenyl)-ethyl]-(R)-4-[(R)-1-[7-(3,4,5-trimethoxy-phenyl)-[1,6]naphthyridin-5-yloxy]-ethyl]-pyrrolidin-2-oneHCID 58072044—

反応条件

温度0 °C

反応手順

114.6 g of powdered 7-(3,4,5-trimethoxy-phenyl)-[1.6]naphthyridine-5-ol is suspended in 900 mL tetrahydrofurane. A solution of 115.9 g of (R)-4-[(S)-1-hydroxyethyl]-1-[(S)-1-(4-methoxyphenyl)-ethyl]-pyrrolidin-2-one and 136 g triphenylphosphine in 1000 mL tetrahydrofurane is added. The suspension is cooled to 0° C. During 40 minutes a solution of 105 mL diisopropylazodicarboxylate [DIAD] in 400 mL tetrahydrofurane is added at 0° C. to 2° C. The suspension is stirred for 3.5 hours at this temperature and then warmed up to 20° C. The solvent is evaporated under reduced pressure. The residue is suspended in 680 mL of tert-butylmethylether. Seeding crystalls of triphenylphosphinoxid are added and the mixture is stirred 16 hours at 20° C. The precipitate is filtered and washed with tert.-butylmethylether. The filtrate is evaporated under reduced pressure. The crude product is dissolved in a mixture of 220 mL of 2-propanol and 1100 mL of isopropyl acetate at 40° C. 48 mL of trimethylchlorosilane are added during 15 minutes. The suspension is stirred for 2 hours at 20° C. The precipitate is filtered and washed with isopropyl acetate and dried at 60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09187478B2
出典データセットuspto-grants-2015_11
ORD IDord-f5a32725ccd24ab2a11fe03b13373d9c
出典メモuspto-grants-2015_11