HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 21444366, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methylpiperazine-1-carbonyl chloride monohydrochloride | HCID 3016934 | — |
| Reactant | 2-(7-Chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-1-isoindolinone | HCID 22754718 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21444366 | HCID 21444366 | 73.5% |
Reaction Steps
Following the procedure of Example 28, but starting from 2-(7-chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-1-isoindolinone (4.8 g.), 1-chlorocarbonyl-4-methyl-piperazine hydrochloride (15.1 g.), triethylamine (14.2 cc., equivalent to 10.2 g.) and pyridine (66 cc.) in methylene chloride (250 cc.), a crude product (7.8 g.) is obtained, which is triturated with water (50 cc.). The solid obtained is filtered off and washed with water (30 cc.). After recrystallisation from isopropanol (240 cc.), 2-(7-chloro1,8-naphthyridin-2-yl)-3-(4-methyl-piperazinyl)carbonyloxy-6-trifluoromethyl-1-isoindolinone (4.7 g.) melting at 219° C is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016274 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-02ca71111948424b80d514902a0b2243 |
| Source note | uspto-grants-1977_04 |