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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176023Generated: November 1, 2026

Trifluoroacetic acid → HCID 90370295, compound

https://huagongshe.com/reaction/2176023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 90370131HCID 90370131—
SolventDichloromethaneHCID 6344—
ProductHCID 90370295HCID 9037029593.6%

Reaction Steps

To a mixture of 8.99 g of tert-butyl 2-({3-[(pentan-3-ylamino)methyl]benzoyl}amino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate and 100 mL of methylene chloride was added 30 mL of TFA, followed by stirring for 15 hours at room temperature. The reaction mixture was concentrated under reduced pressure, and azeotropy was performed using toluene. 4.3 mL of thionyl chloride and 50 mL of toluene were added to the residue, and 0.10 mL of DMF was added dropwise thereto, followed by stirring for 1 hour at 60° C. The reaction mixture was concentrated under reduced pressure, a saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated brined and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:2), thereby obtaining 7.05 g of 2-{3-[(pentan-3-ylamino)methyl]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-cf792b67c6194dd58ab459158576050e
Source noteuspto-grants-2015_06