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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523253Generated: November 3, 2026

Triethylamine → HCID 59627236, compound

https://huagongshe.com/reaction/1523253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 59627203HCID 59627203—
SolventDichloromethaneHCID 6344—
ProductHCID 59627236HCID 5962723695%

Reaction Steps

To a solution of (R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(4-fluorophenyl)-4-(3-hydroxypropyl)tetrahydropyrimidin-2(1H)-one (50 mg, 0.12 mmol) and triethylamine (161 mg, 1.59 mmol) in CH2Cl2 (5 mL) was added methanesulfonyl chloride (91 mg, 0.8 mmol) at 0° C., and the reaction mixture was stirred at rt till the reaction was over. The reaction was quenched with H2O, and the mixture was extracted with EtOAc. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated to give crude 3-((R)-1-((S)-1-(4-bromophenyl)ethyl)-4-(4-fluorophenyl)-2-oxohexahydropyrimidin-4-yl)propyl methanesulfonate (58 mg, 95%), which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079861B2
Source datasetuspto-grants-2015_07
ORD IDord-cbff5c77b238409fa2340d87ce5af3c6
Source noteuspto-grants-2015_07