HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508990Generated: November 1, 2026
Cyclopentanethiol → 4-chloro-2-(cyclopentylthio)-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide
https://huagongshe.com/reaction/1508990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentanethiol | HCID 15510 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide | HCID 90112536 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-chloro-2-(cyclopentylthio)-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide | HCID 90338661 | 86% |
Reaction Steps
To a solution of cyclopentyl mercaptan (0.112 g, 1.10 mmol) in dioxane (4 mL) at rt was added potassium tert-butoxide (0.100 g, 0.88 mmol). The mixture was stirred at rt for 1 h. After this time, 2,4-dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide (0.150 g, 0.74 mmol) in dioxane (1 mL) was added and the mixture was heated to 100° C. for 1 h. Then, the mixture was diluted with methylene chloride and washed with water. The organic layer were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, dichloromethane/methanol) to afford the title compound (0.170 g, 86%) as a brown oil. MW=269.79. 1H NMR (CDCl3, 500 MHz) δ 6.99 (s, 1H) 3.60-3.52 (m, 1H), 3.22 (t, J=7.5 Hz, 2H), 3.01 (t, J=7.5 Hz, 2H), 2.26-2.15 (m, 4H), 1.88-1.79 (m, 2H), 1.77-1.64 (m, 4H); APCI MS m/z 270 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09221843B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-203af98f66ac40ec8d35b0c36562b751 |
|---|
| Source note | uspto-grants-2015_12 |
|---|