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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378604Generated: October 30, 2026

Toluene → HCID 59732028, compound

https://huagongshe.com/reaction/2378604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59732020HCID 59732020—
ReactantHCID 67318551HCID 67318551—
SolventDichloromethaneHCID 6344—
ProductHCID 59732028HCID 5973202894%

Reaction Steps

(R)-tert-Butyl 4-amino-2-benzyl-7-methyl-3-oxo-2,3,4,5-tetrahydro-1H-benzo[c]azepin-8-ylcarbamate (155 mg, 0.39 mmol) was dissolved in dichloromethane (10 mL). Aqueous sodium bicarbonate (10 mL) was added to the mixture. A solution of 20% phosgene in toluene (230 μL, 0.43 mmol) was added to the mixture with vigorous stirring. Reaction stirred at room temperature for 20 minutes. 4-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl) piperidine acetate (140 mg, 0.48 mmol) was added to the mixture. Reaction stirred at room temperature for 1 hour. Reaction layers were partitioned. Organic layer was washed successively with 1N hydrochloric acid and brine. Organic was dried (magnesium sulfate), filtered and concentrated in vacuo. Title compound was obtained as off-white solid in 94% yield. MS m/e (M+H)+=653.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470679B2
Source datasetuspto-grants-2008_12
ORD IDord-2598effc0bb34fc4b7ba87c5b21c2b11
Source noteuspto-grants-2008_12