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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170538Generated: November 1, 2026

Trifluoroacetic acid → HCID 58654424, compound

https://huagongshe.com/reaction/1170538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 58654334HCID 58654334—
SolventDichloromethaneHCID 6344—
ProductHCID 58654424HCID 5865442443.2%

Reaction Steps

2,2,2-Trifluoroacetic acid (20.0 mL, 269 mmol) was added dropwise over 5 minutes to a 0° C. solution of tert-butyl 2-(2-(1H-imidazol-1-yl)-6-methylpyrimidin-4-yl)-3-(methylcarbamoyl)pyrrolidine-1-carboxylate (720 mg, 1.86 mmol) in CH2Cl2 (20 mL). The reaction mixture was warmed to rt over 30 minutes then brought to pH=8 with Na2CO3 (400 mL, sat. aqueous solution). The mixture was extracted with CH2Cl2 (5×30 mL), the combined organic layers were dried over Na2SO4, filtered and concentrated under vacuum to afford 2-(2-(1H-imidazol-1-yl)-6-methylpyrimidin-4-yl)-N-methylpyrrolidine-3-carboxamide (230 mg, 43%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825256B2
Source datasetuspto-grants-2010_11
ORD IDord-12912190070f4151bd9aed9a47a8eea1
Source noteuspto-grants-2010_11