戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 430657作成日:2026年10月25日

Triphenylphosphine → 8-Azidomethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepine

https://huagongshe.com/reaction/430657

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Hydrazoic acidHCID 24530—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物8-Hydroxymethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 18183191—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物8-Azidomethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepineHCID 1818312968%

反応手順

A solution of 3.06 g (9.0 mmol) of 8-hydroxymethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepine (starting compound III.) and 2.58 g (9.9 mmol) of triphenylphosphine in 100 ml of dry tetrahydrofuran is mixed with 13.5 ml of a 1.2N hydrazoic acid solution in toluene, then a solution of 1.74 ml (9.9 mmol) of azodicarboxylic acid-diethyl ester is added, and the mixture is stirred for another 2 hours. The precipitated product is suctioned off and washed with tetrahydrofuran and n-hexane. 2.23 g (68%) of the title compound with a melting point of 198-200° C. is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323197B1
出典データセットuspto-grants-2001_11
ORD IDord-5a7bcb3948914d8b87e3c6b7bab9dfd1
出典メモuspto-grants-2001_11