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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811751Generated: October 30, 2026

Trifluoroacetic acid → HCID 86639753, compound

https://huagongshe.com/reaction/1811751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59224655HCID 59224655—
SolventDichloromethaneHCID 6344—
ProductHCID 86639753HCID 86639753—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-{2-Amino-6-[2-(2,4-bis-tert-butoxycarbonylaminobutyrylamino)ethylsulfanyl]pyrimidin-4-yl}-2,4-dimethylbenzoic acid tert-butyl ester obtained in Step 2 above was dissolved in dichloromethane (37 ml). After the solution was cooled to 0° C., trifluoroacetic acid (13 ml) was added thereto. The reaction solution was gradually warmed to room temperature, and then stirred at room temperature for six hours. After the solvent was distilled off under reduced pressure, dichloromethane (10 ml) was added to the residue and again concentrated under reduced pressure. The resulting residue was suspended in ethyl acetate (60 ml). After the suspension was stirred at room temperature for two hours, the insoluble material was collected by filtration. The obtained solid was dried under reduced pressure to yield 5-{2-amino-6-[2-(2,4-diaminobutyrylamino)ethylsulfanyl]pyrimidin-4-yl}-2,4-dimethylbenzoic acid tert-butyl ester tri(trifluoroacetate) (3.6 g) as a white solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-d92bbb40bbdd420b91ee718935d07930
Source noteuspto-grants-2013_01