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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887908Generated: October 30, 2026

2-Chloro-4,5-difluorobenzoyl Isocyanate → 1-(2-Chloro-4,5-difluorobenzoyl)-3-(6-methoxy-2,4-dioxo-1,2,3,4-tetrahydro-quinazolin-7-yl)urea

https://huagongshe.com/reaction/887908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,5-difluorobenzoyl IsocyanateHCID 11557583—
Reactant7-Amino-6-methoxyquinazoline-2,4(1H,3H)-dioneHCID 68805129—
SolventAcetonitrileHCID 6342—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(2-Chloro-4,5-difluorobenzoyl)-3-(6-methoxy-2,4-dioxo-1,2,3,4-tetrahydro-quinazolin-7-yl)ureaHCID 6909852030%

Reaction Steps

100 mg (0.53 mmol) of 7-amino-6-methoxy-1H-quinazoline-2,4-dione were suspended in 20 ml of acetonitrile and 2 ml of N-methyl-2-pyrrolidinone, and 200 mg (0.97 mmol) of 2-chloro-4,5-difluorobenzoyl isocyanate (example 1a) were added. The reaction mixture was heated to boiling and then quenched with methanol and concentrated in vacuo. The residue was stirred with acetonitrile, and the resulting precipitate was filtered off. 64 mg (30%) of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247452B2
Source datasetuspto-grants-2012_08
ORD IDord-9bc5c7779db4419bb87886b92011092f
Source noteuspto-grants-2012_08