HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-bromo-7-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-Bromo-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide | HCID 11506754 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-7-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 67843076 | — |
Reaction Steps
To a solution of 3-bromo-6,7-dihydro-5H-[1]pyrindine N-Oxide (250 mg, 1.17 mM) in 3 mL of CH2Cl2 at room temperature was added POCl3 (0.131 mL, 1.4 mM) and triethylamine (0.202 mL, 1.4 mM). The reaction was stirred at room temperature for 2 hours then was extracted from saturated NaHCO3 solution into ethyl acetate, washed with saturated NaCl, dried over MgSO4, filtered, and concentrated to dryness. The product was used crude in the next step. 1H NMR (CDCl3): d 8.60 (s, 1 H), 7.80 (s, 1 H), 5.40 (d, 1 H), 3.00 (m, 2 H), 2.20 (m, 2 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05338740 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-808d67f9156c4dc2916c1831155253bd |
| Source note | uspto-grants-1994_08 |