HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl 4-((3-chloro-4-methoxy-phenyl)methylamino)-2-((2S)-2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Prolinol | HCID 640091 | — |
| Reactant | Ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-(methylsulfinyl)pyrimidine-5-carboxylate | HCID 22665570 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-((3-chloro-4-methoxy-phenyl)methylamino)-2-((2S)-2-(hydroxymethyl)pyrrolidin-1-yl)pyrimidine-5-carboxylate | HCID 52348789 | — |
Reaction Steps
In the solution of ethyl 4-((3-chloro-4-methoxybenzyl)amino)-2-methanesulfinyl-5-pyrimidine carboxylate in DCM was added triethylamine (4.24 g, 42 mmol). The mixture was cooled in an ice bath, then was added L-prolinol (2.2 g, 19.8 mmol) dropwise. The reaction mixture was stirred at ambient temperature for 3 h. The reaction was monitored by LC-MS. After the completion of the reaction, the reaction mixture was washed with water, dilute hydrochloric acid, sodium bicarbonate aqueous solution and brine, each once. The organic phase was dried over sodium sulfate and concentrated until the solvent was removed. The product was used in subsequent procedures without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359371B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-999584349d1649d9b9b99a7f1263b864 |
| Source note | uspto-grants-2016_06 |