HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → HCID 58760954, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86594821 | HCID 86594821 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 58760954 | HCID 58760954 | 57% |
Reaction Steps
A solution of 2-(4-chloro-phenyl)-1-(2-fluoro-phenyl)-5-formyl-1H-imidazole-4-carboxylic acid ethyl ester I-5e-2 (1000 mg, 2.68 mmol), cyclopentylamine (251 mg, 2.95 mmol), NaBH(OAc)3 (796 mg, 3.76 mmol) in dichloroethane was stirred for 17 h at room temperature. The reaction was concentrated in vacuo and the residue was diluted with CHCl3. The organic solution was washed with sat'd aq. NaHCO3 and sat'd aq. NaCl, dried, and concentrated under vacuum. The crude residue was purified on SiO2-gel (Flash 40s) using a solvent gradient of 30% EtOAc/hexanes to 80% EtOAc/hexanes to give the desired product (I-5f) as a yellow oil (680 mg, 57%): +APCI MS (M+1) 442.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07145012B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-74985de3c0c3480888b83c0ff66eb9da |
| Source note | uspto-grants-2006_12 |