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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273077Generated: November 1, 2026

Phenyl chloroformate → HCID 89714526, compound

https://huagongshe.com/reaction/2273077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Difluoromethoxy)anilineHCID 2774110—
ReactantHCID 89714581HCID 89714581—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89714526HCID 89714526124.4%

Reaction Steps

96.84 mg of 3-difluoromethoxyphenylamine (590.31 μmol), 206.20 μl of DIEA (1.18 mmol) and 30.81 μl of phenyl choroformate (237.83 μmol) are added to 4 ml of THF in a microwave tube. The mixture is stirred at room temperature for 20 minutes. 250 mg of 4-(4-aminophenyl)-6-ethyl-8,8-dimethyl-2-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-7,8-dihydro-6H-9-oxa-1,3,6-triazabenzocyclohepten-5-one (590.31 μmol) are added and the resulting mixture is heated for 1 hour at 120° C. in a Biotage microwave machine. The reaction medium is evaporated under reduced pressure. The residue is chromatographed on silica gel, eluting with a DCM/MeOH mixture from (100/0 v/v) up to (98/2 v/v) to give 180 mg of 1-(3-difluoromethoxyphenyl)-3-{4-[6-ethyl-8,8-dimethyl-2-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-5-oxo-5,6,7,8-tetrahydro-9-oxa-1,3,6-triazabenzocyclohepten-4-yl]phenyl}urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120812B2
Source datasetuspto-grants-2015_09
ORD IDord-637fa3637353482c966ad497c8bb1b13
Source noteuspto-grants-2015_09