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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942507Generated: October 31, 2026

Benzyl Bromide → HCID 67330354, compound

https://huagongshe.com/reaction/1942507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 67330115HCID 67330115—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
ProductHCID 67330354HCID 67330354—

Reaction Steps

To a solution of ethyl 4-(2-{[(benzyloxy)carbonyl]amino}ethyl)-6-{[[(3R)-1-(tert-butoxycarbonyl)piperidin-3-yl](isopropyl)amino]carbonyl}-2-methyl-3-oxo-7-(trifluoromethyl)-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate (1.00 g) in N,N-dimethylacetamide (2.7 ml) was added at 0° C. benzyl bromide (0.794 ml), and sodium hydride (193 mg), and the mixture was stirred for one hour. To the reaction solution were added 2N-aqueous sodium hydroxide solution (5.36 ml) and tetrahydrofuran (5.0 ml), and the mixture was stirred at room temperature for one hour. To the reaction solution was added a 5% aqueous potassium hydrogen sulfate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform /methanol=100/3, containing 5% acetic acid) to give the title compound (0.800 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-6b43720b9f0149b08fa3607aa809dd86
Source noteuspto-grants-2013_03