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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430657생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/430657

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Hydrazoic acidHCID 24530—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물8-Hydroxymethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 18183191—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물8-Azidomethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepineHCID 1818312968%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323197B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-5a7bcb3948914d8b87e3c6b7bab9dfd1
출처 메모uspto-grants-2001_11