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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379538Generated: October 30, 2026

Carbon Dioxide → HCID 10955701, compound

https://huagongshe.com/reaction/379538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57140763HCID 57140763—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10955701HCID 10955701—

Reaction Steps

20.7 g (0.61 mmol) of 4-(tert-butoxycarbonylpiperidin-4-ylamino)-5-chloro-6-ethylpyrimidine (Example A) were dissolved in 100 ml of dichloroethane and 148.0 g of trifluorocetic acid were added slowly. After the evolution of CO2 had ceased, stirring was continued for 2 more hours. After the solvent and the trifluoroacetic acid had been stripped off, the mixture was concentrated and the residue was taken up in dichloromethane/water. After the mixture had been rendered weakly alkaline by addition of dilute sodium hydroxide solution, the organic phase was separated off, dried and concentrated. This gave 12.3 g (83.9% of theory) of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300333B1
Source datasetuspto-grants-2001_10
ORD IDord-978f022d57634d4099667714e1b0a7b4
Source noteuspto-grants-2001_10