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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186101Generated: October 31, 2026

Phosphorus oxychloride → Benzodiazepine

https://huagongshe.com/reaction/1186101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantBenzimidazol-2-oneHCID 162542—
ReactantHCID 54405697HCID 54405697—
ProductBenzodiazepineHCID 134664—

Reaction Steps

The title compound was prepared according to the procedures shown in the scheme below. Compound 5-chloroisatoic anhydride (A) was reacted with (R)-2-chlorophenylalanine to provide benzodiazepine-dione B based on procedures described in, for instance, Example 2. Reaction of benzodiazepine-dione B with para-methoxybenzyl chloride in the presence of base, according to procedures described in, for instance, Example 3, provided PMB-protected benzodiazepine-dione C. Conversion of benzodiazepine-dione C to imidoyl chloride D was accomplished using phosphorous oxychloride, based on procedures described in, for instance, Example 4. The benzimidazolone substituent was installed using Suzuki coupling, based on procedures described in, for instance, Example 7, to provide benzodiazepine E. Removal of the PMB protecting group was accomplished by reacting benzodiazepine E with AlCl3, based on procedures described in, for instance, Example 8, to provide benzodiazepine F.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673897B2
Source datasetuspto-grants-2014_03
ORD IDord-a2993a88cd154d00ba98492430b875df
Source noteuspto-grants-2014_03