HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 58662432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 58662450 | HCID 58662450 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58662432 | HCID 58662432 | 96.5% |
Reaction Steps
To a stirred solution of [(3,5-Bis-trifluoromethyl-benzylidene)-amino]-6-ethyl-1,3-dimethyl-1,4,5,6-tetrahydro-pyrazolo[3,4-b]pyridine-7-carboxylic acid ethyl ester (0.19 g, 0.04 mmol) obtained in step (v), in 10 mL of methanol was added sodium cyanoborohydride (0.078 g, 0.12 mmol). This reaction mixture was stirring for around 3 hours at room temperature, after which time the methanol was evaporated from the solution to afford a crude residue. Water was added to this residue, and the product was extracted with ethyl acetate (3×10 mL). The organic solvent was dried over sodium sulfate, filtered, and the solvent was evaporated from the filtrate under vacuum to provide the desired amine compound (0.019 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700774B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-6a9fbbba39dc4fa1ab8a3ad8cf076293 |
| Source note | uspto-grants-2010_04 |