HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20262398, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(6-chloro-pyridine-3-sulfonyl)-morpholine | HCID 274147 | — |
| Reactant | HCID 70042414 | HCID 70042414 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20262398 | HCID 20262398 | 20.2% |
Reaction Steps
A solution of 2-(2-aminoethyl)-5-{[4-(2,3-dichlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridin-2-yl]methoxymethyl}tetrazole (0.33 g), 2-chloro-5-(4-morpholinylsulphonyl)pyridine (145 mg) and triethylamine (65 mg) in dichloromethane (15 ml) was heated under reflux for 2 hours, then stirred at room temperature for 16 hours and evaporated. The residue was purified by chromatography on silica (6 g) using dichloromethane plus from 0 to 5% by volume of methanol as eluant. Appropriate fractions were combined and evaporated to give the title compound (84 mg), m.p. 112°-114° C. Found: C,56.32; H,5.90; N,10.45. C31H36Cl2N8O8S requires: C,56.13; H,5.80; N,10.48%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04548935 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-7f61f9a32cc944c8b0332f2fec1a90b7 |
| Source note | uspto-grants-1985_10 |