HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 13823460, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(4-Bromobutyl)-4-hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-one | HCID 54716551 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13823460 | HCID 13823460 | — |
Reaction Steps
A suspension of 3-(4-bromobutyl)-4-hydroxy-1-Phenyl-1,8-naphthyridin-2(1H)one (5g.) in methylene chloride (350 ml.), in an atmosphere of nitrogen, was stirred at room temperature and to it was added triethylamine (4.1 ml.). The mixture was stirred at room temperature for 16 hrs. Water (300 ml.) was added and the aqueous layer was adjusted to pH 4.5 with hydrochloric acid. The organic layer was separated and the aqueous layer was back-extracted with methylene chloride. The combined organic layers were washed with water, dried (Na2SO4) , filtered and evaporated to yield a solid which was recrystallized from-isopropanol to yield 1'-phenylspiro[cyclopentane-1,3'-(1,8) naphthyridine]2',4'-(1'H)dione, m.p. 178°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05350755 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-47d3892c4ad9478dab7a9caeb71fb7c7 |
| Source note | uspto-grants-1994_09 |