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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631707Generated: November 3, 2026

4-(Methylsulfonyl)benzyl Bromide → (R)-2-chloro-5-(4-(methylsulfonyl)benzyl)-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine

https://huagongshe.com/reaction/1631707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methylsulfonyl)benzyl BromideHCID 2733581—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant(R)-2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridineHCID 86670088—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(R)-2-chloro-5-(4-(methylsulfonyl)benzyl)-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridineHCID 8667009332.1%

Reaction Steps

4-Methylsulphonylbenzyl bromide (121 mg, 0.485 mmol) was added to a mixture of (R)-2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine (PREPARATION x3, 100 mg, 0.441 mmol) and potassium tert-butoxide (59.4 mg, 0.529 mmol) in DMSO (2206 μL) at room temperature. The resultant mixture was stirred overnight at room temperature and subsequently diluted with EtOAc and water. The mixture was extracted twice with EtOAc. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, eluting with 0-10% MeOH/CHCl3 gradient) to afford the title compound as an off-white solid (55.9 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791107B2
Source datasetuspto-grants-2014_07
ORD IDord-a18568e81cd44fb280f17ca70a89c430
Source noteuspto-grants-2014_07