HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040107Generated: October 31, 2026
Trifluoroacetic acid → HCID 178489242, compound
https://huagongshe.com/reaction/2040107
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178489243 | HCID 178489243 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178489242 | HCID 178489242 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580832B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-923a3678257240689c14a56cf8bc160f |
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| Source note | uspto-grants-2013_11 |
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