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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353038Generated: October 29, 2026

HCID 21962576, compound → HCID 21962570, compound

https://huagongshe.com/reaction/353038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21962576HCID 21962576—
CatalystTitanium TetrachlorideHCID 24193—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21962570HCID 21962570—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of titanium (IV) chloride in tetrahydrofuran under nitrogen atmosphere, is added and equimolar amount of stannous chloride dihydrate, and the mixture is stirred 1 hour at room temperature. Then, a solution of ethyl 3-[(4-{3-[N-benzyloxycarbonyl-N-(1-oxido-2-pyridinyl)amino]propyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)sulfanyl]-3-phenylpropanoate is added and the mixture heated 3 hours at 40° C. After evaporation of the solvent, ice and aqueous sodium bicarbonate are added, the mixture extracted with ethyl acetate, and the organic layers are combined and dried over sodium sulfate. The solvent is evaporated and ethyl 3-[(4-{3-[N-benzyloxycarbonyl-N-(2-pyridinyl)amino]-propyl}-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)sulfanyl]-3-phenylpropanoate is isolated by column chromatography. A solution of ethyl 3-[(4-{3-[N-benzyloxycarbonyl-N-(2-pyridinyl)amino]-propyl)-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-7-yl)sulfanyl]-3-phenylpropanoate in acetic acid is treated with a solution of 30% hydrobromic acid in acetic acid at room temperature overnight. The solvent is evaporated under reduced pressure, and the residue is treated with a saturated sodium bicarbonate solution. The aqueous mixture is extracted with dichloromethane. The organic extracts are dried over sodium sulfate, evaporated to small volume and the product is purified by flash chromatography

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750215B2
Source datasetuspto-grants-2004_06
ORD IDord-f21d90609d8b444c905ca7549f1ddd9c
Source noteuspto-grants-2004_06