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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516264Generated: October 29, 2026

Sodium Bicarbonate → HCID 66982715, compound

https://huagongshe.com/reaction/516264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86658952HCID 86658952—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66982715HCID 66982715—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 400 mg of t-butyl 5-cyclopropyl-4-[(2R)-2-methoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propyl]-3,4,6,7,9,10-hexahydro[1,4]oxazino[2,3-h][3]benzazepine-8(2H)-carboxylate was added 7 ml of a 1 M solution of tetrabutylammonium fluoride in THF, followed by heating and stirring at 60° C. for 13 hours under an argon atmosphere. The reaction mixture was cooled to room temperature and a saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with ethyl acetate twice. The combined organic layer was dried over anhydrous sodium sulfate and then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: HEX-EtOAc) to obtain 257 mg of t-butyl 5-cyclopropyl-4-[(2R)-3-fluoro-2-methoxypropyl]-3,4,6,7,9,10-hexahydro[1,4]oxazino[2,3-h][3]benzazepine-8(2H)-carboxylate as a white foamed solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108977B2
Source datasetuspto-grants-2015_08
ORD IDord-37134a41e3524aae80ad6f47c73b35ce
Source noteuspto-grants-2015_08