HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Ethyl 2-amino-4-(propylamino)pyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Methylthio-4-propylamino-5-pyrimidine carboxylic acid ethyl ester | HCID 10562975 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | m-Chloroperbenzoic acid | HCID 70297 | — |
| Product | Ethyl 2-amino-4-(propylamino)pyrimidine-5-carboxylate | HCID 90052100 | — |
Reaction Steps
To a solution of 2-(methylthio)-4-(propylamino)pyrimidine-5-carboxylic acid ethyl ester (A1, 11.7 g) in N-methylpyrrolidone (90 mL), meta-chloroperbenzoic acid (70 to 75% wt, 20.8 g) was added under ice cooling, and the mixture was stirred at room temperature for 40 minutes. To the reaction mixture, N,N-diisopropylethylamine (23.9 mL) and 10% aqueous ammonia (60.0 mL) were added at room temperature, and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was poured into water (400 mL). The solid matter was taken by filtration, washed with water, and then dried under reduced pressure to obtain ethyl 2-amino-4-(propylamino)pyrimidine-5-carboxylate (C3, 8.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145415B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-1419957473094188ad1fcf531775181f |
| Source note | uspto-grants-2015_09 |