HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290320Generated: October 31, 2026
Ammonium Hydroxide → HCID 13457209, compound
https://huagongshe.com/reaction/2290320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 13457207 | HCID 13457207 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13457209 | HCID 13457209 | — |
Reaction Steps
A mixture of 2-{[4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridin-2-yl]methoxymethyl}-4-ethoxycarbonylthiazole (0.54 g), dioxane (20 ml) and 0.880 aqueous ammonium hydroxide solution (20 ml) was stirred at room temperature for 43 hours and then evaporated. The residue was partitioned between ethyl acetate and water and the organic layer washed with water, dried (Na2SO4) and evaporated. The residual oil was purified by chromatography on silica (t.l.c. grade, 10 g) using dichloromethane plus 0-3% v/v methanol as eluant. Appropriate fractions were combined and evaporated and the residual oil triturated with diethyl ether. The resulting solid was collected, washed with diethyl ether and dried to give the title compound (0.30 g) as a monohydrate, m.p. 160°-164° C. decomp.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04616024 |
|---|
| Source dataset | uspto-grants-1986_10 |
|---|
| ORD ID | ord-6f4d37845d9a417085b7ddea47fa93e0 |
|---|
| Source note | uspto-grants-1986_10 |
|---|