HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 10955701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57140763 | HCID 57140763 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 10955701 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300333B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-978f022d57634d4099667714e1b0a7b4 |
| Source note | uspto-grants-2001_10 |