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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359575Generated: October 25, 2026

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

https://huagongshe.com/reaction/1359575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHydrazoic acidHCID 24530—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant8-Hydroxymethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepineHCID 18183191—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product8-Azidomethyl-5-(4-nitrophenyl)-9H-1,3-dioxolo[4,5-h][2,3]-benzodiazepineHCID 1818312968%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600036B2
Source datasetuspto-grants-2003_07
ORD IDord-a4eed99740a94f23ba49a5f799c139d2
Source noteuspto-grants-2003_07