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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244101Generated: November 1, 2026

Phosgene → HCID 136105446, compound

https://huagongshe.com/reaction/2244101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantIsobutylamineHCID 6558—
ReactantHCID 66850173HCID 66850173—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136105446HCID 13610544666.7%

Reaction Steps

To a stirring solution of 1-[2-(2-Methoxyphenyl)-7-methylquinazolin-4-yl]-piperidin-4-ol (100 mg, 0.30 mmol) and THF (500 μL) under N2, was added phosgene (317 μL, 0.60 mmol, 20% in toluene). The mixture was stirred at room temperature for 15 minutes. Isobutylamine (300 μL, 3.0 mmol) was added dropwise over a 2 minute period followed by stirring at room temperature for 1 hour. The mixture was evaporated to dryness and the obtained residue was purified via silica gel chromatography using 97% CH2Cl2/3% MeOH to obtain the desired carbamate intermediate as a clear oil (90 mg, 0.20 mmol). To a stirring solution of the carbamate intermediate (90 mg, 0.20 mmol) and CH2Cl2 (15 mL), under N2, at −78° C., was added BBr3 (0.60 mL, 0.60 mmol, 1.0 M in CH2Cl2) dropwise over a period of 2 minutes. The mixture was then allowed to warm to room temperature and was then heated at 50° C. for 15 minutes. The mixture was poured into a saturated aqueous NaHCO3 solution (80 mL) and the organic portion was evaporated to dryness. The residue was purified via HPLC to obtain the desired carbamate as a TFA salt (66 mg, 0.12 mmol, 39% yield). LC/MS (10-99%) M/Z 435.3 retention time 3.08 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678802B2
Source datasetuspto-grants-2010_03
ORD IDord-0c4f6ca488324effab510f00c0d58edd
Source noteuspto-grants-2010_03