HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 15454675, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 2-(Chloromethyl)-3-methylpyridine hydrochloride | HCID 13058683 | — |
| Reactant | HCID 178505405 | HCID 178505405 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15454675 | HCID 15454675 | 154.4% |
Reaction Steps
The title compound (0.95 g, 63%) was prepared by the general procedure using, 6-fluoro-5-(piperidin-1-yl)-2-mercapto-1H-benzimidazole (0.70 g, 2.8 mmol) (obtained in preparation 3), 4-(piperidin-1-yl)-3 )-methyl-2-chloromethylpyridine hydrochloride (0.91 g, 3.5 mmol), sodium hydroxide (0.30 g, , 7.7 mmol) and ethanol (15 mL). mp 161-162° C.; IR (KBr) 3430, 1581, 1429 cm-1 ; 1H NMR (CDCl3) δ 1.60 (m, 4H, 2×CH2), 1.74 (m, 8H, 2×(CH2)2), 2.30 (s, 3)H, CH3), 3.00 (m, 8H, 2×N(CH2)2), 4.32 (s, 2H, SCH2), 6.82 (d, J=5.4 Hz, 1H), 7.12 (d, J=7.7 Hz, 1H), 7.24 (d, J=12.1 Hz, 1H), 8.28 (d, J=5.5 Hz, 1H); Mass (m/z) 439 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051570 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-894933d3454b46df8b5a612aae6466ef |
| Source note | uspto-grants-2000_04 |