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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176031Generated: November 1, 2026

Thionyl Chloride → HCID 90370056, compound

https://huagongshe.com/reaction/2176031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 90370047HCID 90370047—
SolventTolueneHCID 1140—
ProductHCID 90370056HCID 9037005689.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 22.2 g of 2-{[3-(morpholin-4-ylmethyl)benzoyl]amino}-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid and 230 mL of toluene was heated at 60° C., and 20 mL of thionyl chloride was added thereto, followed by stirring for 1 hour at 60° C. The insoluble material was collected by filtration and washed with toluene. A saturated aqueous sodium hydrogen carbonate solution and ethyl acetate were added to the material collected by filtration, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was washed with ethanol, thereby obtaining 18.9 g of 2-[3-(morpholin-4-ylmethyl)phenyl]-5,6,7,8-tetrahydro-4H-[1]benzothieno[2,3-d][1,3]oxazin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062032B2
Source datasetuspto-grants-2015_06
ORD IDord-55ef6bd9cd84435a8ce0f92b518dc6a4
Source noteuspto-grants-2015_06