HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → 5-chloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 3-Amino-6-bis(ethoxycarbonyl)methyl-2-chloropyridine | HCID 10517360 | — |
| Reactant | 3-Amino-2-bis(ethoxycarbonyl)methyl-6-chloropyridine | HCID 10589329 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5-chloro-1H-pyrrolo[3,2-b]pyridin-2(3H)-one | HCID 10654688 | — |
Reaction Steps
The mixture containing 3-amino-2-bis(ethoxycarbonyl)methyl-6-chloropyridine, 3-amino-6-bis(ethoxycarbonyl)methyl-2-chloropyridine and diethyl malonate was taken up in 6N HCl solution (700 mL) and heated at reflux for 5 hours. After removing the aqueous acid in vacuo, the residue was taken up in water and again concentrated to yield 5-chloro-4-azaoxindole as a brown solid which was dried in the air. The yield was 7.04 g. (32% overall from 2,6-dichloro-3-nitropyridine). An analytical sample was prepared by recrystallization from isopropanol; m.p. 250°-254° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811432 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-040800c009b843f88f1782ad86d73ea9 |
| Source note | uspto-grants-1998_09 |