HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 21537687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21537693 | HCID 21537693 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21537687 | HCID 21537687 | — |
Reaction Steps
A mixture of 15.3 g. of 6-ethoxy-1-ethyl-1H-pyrazolo-[3,4-b]pyrazine-5-carbonyl chloride (0.06 mol.), 6.6 g. of 2-amino-thiazole (0.66 mol.) and 9.1 ml. of triethylamine (0.66 mol.) in 400 ml. of dry benzene are refluxed for 21/2 hours. After cooling the reaction mixture, the precipitated triethylamine hydrochloride is filtered off and the filtrate is evaporated to dryness. The crude 6-ethoxy-1-ethyl -N-2-thiazolyl-1H-pyrazolo-[3,4-b]pyrazine-5-carboxamide is recrystallized from ethyl acetate, m.p. 151°-152°, yield 9.9 g. (52 %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957782 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-ba47830736cb4a2fa5ca644b05f9ce97 |
| Source note | uspto-grants-1976_05 |