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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537534Generated: October 30, 2026

Trifluoroacetic acid → HCID 86701432, compound

https://huagongshe.com/reaction/537534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68157032HCID 68157032—
SolventDichloromethaneHCID 6344—
ProductHCID 86701432HCID 86701432—

Reaction Steps

Trifluoroacetic acid (0.30 mL) was added to a solution of tert-butyl 3-(2-(cyclohexyl(6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridine-3-yl)methylamino)nicotinamido)propanoate (30 mg, 0.052 mmol) in dichloromethane (0.4 mL). The mixture was stirred at room temperature for 2 hours. The reaction was concentrated and the residue was co-evaporated with dichloromethane, ethyl acetate and toluene several times, to give (+/−)-3-(2-(cyclohexyl(4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)methylamino)nicotinamido)propenoic acid, as a solid. 1H NMR (400 MHz, CDCl3, δ): 9.81 (br. s, 1H), 8.94 (hr. s, 1H), 8.31-8.21 (m, 1H), 8.15 (s, 1H), 7.87 (s, 1H), 7.66 (d, J=8.58 Hz, 2H), 7.61-7.51 (m, 1H), 7.39 (d, J=8.39 Hz, 2H), 6.70-6.58 (m, 1H), 4.29-4.17 (m, 1H), 3.69-3.53 (m, 2H), 2.76-2.65 (m, 2H), 2.00-0.91 (m, 11H). MS (M+1): 516.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859591B2
Source datasetuspto-grants-2014_10
ORD IDord-f24168ef5cd447c1bda14cec13ff2dce
Source noteuspto-grants-2014_10