HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentylamine → HCID 17838262, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentylamine | HCID 8060 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(1H-5-Indazolylamino)-1-cyclohexanone | HCID 17838271 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 17838262 | HCID 17838262 | 13.4% |
Reaction Steps
4-(1H-5-Indazolylamino)-1-cyclohexanone (intermediate 3) (57 mg) and amylamine (44 mg) were dissolved in methanol (1 ml), and sodium triacetoxyborohydride (105 mg) was added by portions to the solution at room temperature. The reaction mixture was stirred at room temperature for 18 hr. Hydrochloric acid-methanol was then added thereto, and the reaction mixture was stirred and was then concentrated. The residue was purified by HPLC [0.5% aqueous trifluoroacetic acid solution/acetonitrile] to give an anti-form compound (10 mg) and a syn-form compound (10 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217722B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-f76352db80254a8aa209109521c494cc |
| Source note | uspto-grants-2007_05 |