HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 3-Ethoxycarbonyl-1-(2-fluorbenzyl)-1H-pyrazolo-(3,4,5)-pyridin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N,N-Dimethylacrylamide | HCID 17587 | — |
| Reactant | ethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate | HCID 11391384 | — |
| Product | 3-Ethoxycarbonyl-1-(2-fluorbenzyl)-1H-pyrazolo-(3,4,5)-pyridin | HCID 11162345 | — |
Reaction Steps
The solution obtained from 2A) is mixed with 61.25 ml (60.77 g, 0.613 mmol) of dimethylaminoacrolein and 56.28 ml (83.88 g, 0.736 mol) of trifluoroacetic acid and boiled under argon for 3 days. The solvent is then evaporated in vacuo, and the residue is added to 2 l of water and extracted three times with 1 l of ethyl acetate each time. The combined organic phases are dried over magnesium sulfate and concentrated in a rotary evaporator. Chromatography is carried out on 2.5 kg of silica gel, eluting with a toluene/toluene-ethyl acetate=4:1 gradient. Yield: 91.6 g (49.9% of theory over two stages).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105523B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-69fe3f9a36c74fe6bc4a4bbdc28675d6 |
| Source note | uspto-grants-2006_09 |