HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 18946789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 18946789 | HCID 18946789 | 88.2% |
Reaction Steps
To 40 ml of n-butyl alcohol was added 1.18 g of 7-azaindole, 0.88 g of dimethylamine hydrochloride and 0.33 g of paraformaldehyde, and the mixture refluxed for 30 minutes. The clear solution was then evaporated to dryness in vacuo, and 10 ml of 10% aqueous hydrochloric acid was added to the residue. The water layer was extracted with ether, and then made strongly basic with potassium carbonate. The resulting precipitate was filtered off, washed with ether and dried, yielding 1.42 g (81.1%) of 3-dimethylamino-7-azaindole, m.p. 144°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380739 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-682775b56be642198c6b2debcc89c777 |
| Source note | uspto-grants-1995_01 |