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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023561Generated: November 1, 2026

Trifluoroacetic acid → HCID 67235668, compound

https://huagongshe.com/reaction/1023561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86673596HCID 86673596—
SolventDichloromethaneHCID 6344—
ProductHCID 67235668HCID 67235668—

Reaction Steps

In a 50 mL round-bottomed flask 1,1-dimethylethyl[2-({6-[(2,6-dimethylphenyl)oxy]-3-pyridinyl}amino)-1,1-dimethyl-2-oxoethyl]carbamate (Intermediate 79, 202.1 mg) was dissolved in dichloromethane (2 mL) to give a pale yellow solution. Trifluoroacetic acid (2 mL, 26.0 mmol) was added. The reaction mixture was stirred at room temperature for 20 minutes. The solvent was evaporated under vacuum to afford a yellow oil which was charged on a 5 g SCX cartridge. It was then flushed with 25 mL of MeOH followed by 25 mL of 2M solution of ammonia in MeOH. The ammonia eluate was evaporated under vacuum to afford the title compound as a yellow oil which solidified (144.4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722695B2
Source datasetuspto-grants-2014_05
ORD IDord-e23f3efa40c048758205d62f33716405
Source noteuspto-grants-2014_05