HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Ethylbenzylamine → HCID 67710926, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Ethylbenzylamine | HCID 84352 | — |
| Reactant | HCID 22911180 | HCID 22911180 | — |
| Product | HCID 67710926 | HCID 67710926 | — |
Reaction Steps
2-{3-Chloro-4-[N-(2-chloroethyl)-N-methylamino]-2-pyridyl}-methylthio-1H-benzimidazole (500 mg/1.24 mmol) are heated in N-ethylbenzylamine (15 ml) at 140° C. for 4.5 h. Then the excess N-ethylbenzylamine is removed by distillation under high vacuum, and the residue is chromatographed on silica gel (dichloromethane/methanol 97/3 mixture which contains 1 ml of conc. NH3 ×aq./l). The collected pure fractions are concentrated together in vacuo and dissolved in a little methanol, and saturated ethereal hydrochloric acid (1 ml) and diisopropyl ether are added and the solid which precipitates thereby is filtered off and dried in vacuo. Yield: 200 mg (28%) of the title compound as a colorless solid of melting point >180° (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05668131 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-15b2229e38f44b4b919c43b1bdb5d9bb |
| Source note | uspto-grants-1997_09 |