HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-[2-(Isopropylamino-methyl)-pyrrolidin-1-yl]-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (R)-isopropyl-pyrrolidin-2-ylmethyl-amine | HCID 11564489 | — |
| Reactant | 2-Chloro-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one | HCID 16115688 | — |
| Reactant | 5-(3-Bromo-phenyl)-2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one | HCID 22185186 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(Isopropylamino-methyl)-pyrrolidin-1-yl]-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one | HCID 22185211 | — |
Reaction Steps
To a 100 mL RBF, was added (R)-isopropyl-pyrrolidin-2-ylmethyl-amine (0.13 g, 0.6 mmol), and 50 mL dichloromethane at 0° C. under nitrogen. 0.28 mL diisopropylethylamine (1.6 mmol) was added drop wise, and stirred for 10 min. 2-Chloro-3-methyl-6-pyridin-4-yl-5-m-tolyl-3H-pyrimidin-4-one (0.16 g, 0.5 mmol) was added in one portion, and stirred at 0° C. to rt for 12 h. (This meta-methyl chloro-intermediate was synthesized by a similar procedure as that of 5-(3-Bromo-phenyl)-2-chloro-3-methyl-6-pyridin-4-yl-3H-pyrimidin-4-one.) The mixture was diluted with 100 mL dichloromethane, washed with sat. NaHCO3 and brine. After purified by flash chromatography, the title compound was obtained in 0.219 g as pale yellow solid. MS (ES+): 418 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026326B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-6ed2ec9ae5184a758d239be3ba870bb0 |
| Source note | uspto-grants-2006_04 |