HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 86714222, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86714221 | HCID 86714221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86714222 | HCID 86714222 | 105.6% |
Reaction Steps
Methyl 4-((4-(4-(tert-butoxycarbonyl)piperazin-1-yl)-3-(trifluoromethyl)phenyl)amino)-6-chloro-1,5-naphthyridine-3-carboxylate (0.565 g, 1.0 mmol) was added to ethanol (10 mL), to the system added sodium borohydride (0.228 g, 6 mmol) in batches, stirred at room temperature for 18 h. Ethanol was removed under reduced pressure, added 10 mL of water, and extracted with 80 mL of dichloromethane. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure to give 0.568 g of a crude solid product. The solid was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284315B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-1d347fa119254d519da5b6e20a0d9daa |
| Source note | uspto-grants-2016_03 |