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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409431Generated: October 30, 2026

Trifluoroacetic acid → HCID 42634257, compound

https://huagongshe.com/reaction/409431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantIsopropyl chloroformateHCID 7917—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 42633526HCID 42633526—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 42634257HCID 4263425773%

Reaction Steps

To a solution of (2R,4S)-4-{(3,5-bis-trifluoromethyl-benzyl)-[5-(1-methyl-1H-pyrazol-4-yl)-pyrimidin-2-yl]-amino}-2-ethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (0.200 mmol; 120 mg) in dichloromethane (2.0 mL) is added trifluoroacetic acid (0.7 mL). The mixture is stirred for 1 hour, and then concentrated under reduced pressure. To a mixture of the obtained residue and N,N-diisopropylethylamine (1.6 mmol; 207 mg) is added isopropyl chloroformate (0.4 mmol; 49 mg). The mixture is stirred for 1 hour at room temperature, and then diluted with water and dichloromethane. The organic layer is separated to concentrated under reduced pressure. The obtained residue is purified by silica gel column chromatography (eluent: n-hexane/EtOAc) to give (2R,4S)-4-{(3,5-Bis-trifluoromethyl-benzyl)-[5-(1-methyl-1H-pyrazol-4-yl)-pyrimidin-2-yl]-amino}-2-ethyl-pyrrolidine-1-carboxylic acid isopropyl ester (51 mg, 73%); ESI-MS m/z: 599 [M+1]+, Retention time 2.15 min (condition A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759365B2
Source datasetuspto-grants-2014_06
ORD IDord-a19fc1f9c551463daff891f691914120
Source noteuspto-grants-2014_06