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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855799Generated: 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/855799

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 numberUS07262220B2
Source datasetuspto-grants-2007_08
ORD IDord-a73a9f8912c54ee1907d6ead7f5b8e2f
Source noteuspto-grants-2007_08