Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040107Generated: October 31, 2026

Trifluoroacetic acid → HCID 178489242, compound

https://huagongshe.com/reaction/2040107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178489243HCID 178489243—
SolventDichloromethaneHCID 6344—
ProductHCID 178489242HCID 17848924263%

Reaction Conditions

Temperature0 °C

Reaction Steps

LC/MS (m/z) [M+1]+618.8 (calculated for C29H29F3N4O6S, 618.63). 2-({5-[4-(4-Cyano-2-trifluoromethyl-phenoxy)-3-methoxy-benzylidene]-4-oxo-4,5-dihydro-thiazol-2-ylamino}-methyl)-morpholine-4-carboxylic acid tert-butyl ester (0.1 g, 0.16 mmol) was dissolved in dry dichloromethane (6 mL). To the reaction mixture was then added at 0° C. trifluoroacetic acid (2 mL). The reaction mixture was stirred at 0° C. for 1 hour and then at room temperature for 30 minutes. The reaction mixture was then partitioned with saturated aqueous sodium bicarbonate and dichloromethane. The organic layer was washed with brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash chromatography (6% ammonia 2.0 M methanol/dichloromethane) to yield the compound as a solid (0.052 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580832B2
Source datasetuspto-grants-2013_11
ORD IDord-923a3678257240689c14a56cf8bc160f
Source noteuspto-grants-2013_11