HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22754754, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(7-Chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-1-isoindolinone | HCID 22754718 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22754754 | HCID 22754754 | — |
Reaction Steps
Pyridine (10 cc.) and butyl isocyanate (11.2 cc.) are added to a suspension of 2-(7-chloro-1,8-naphthyridin-2-yl)-3-hydroxy-6-trifluoromethyl-isoindolin-1-one (3.8 g.) in acetonitrile (380 cc.). The mixture is heated to the reflux temperature and triethylamine (0.5 cc.) is added. Refluxing is continued for 50 minutes until dissolution. After cooling the solution, the precipitate formed is filtered off and washed with water (30 cc.). After drying, a first crop of 2-(7-chloro-1,8-naphthyridin-2-yl)-3-n-butylaminocarbonyloxy-6-trifluoromethyl-isoindolin-1-one (2.8 g.) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04131674 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-48265dc15ee1448e807c41b69845e4ad |
| Source note | uspto-grants-1978_12 |