HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 19030851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18960741 | HCID 18960741 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19030851 | HCID 19030851 | 85% |
Reaction Steps
A mixture (5 ml) of hydrobromic acid and acetic acid (35 % solution) is added to 1-{1-[4-(N-t-butoxycarbonyl-N-methylamino)benzoyl]-4-piperidinyl}-3,4-dihyrocarbostyril (1.8 g) and the mixture is stirred at room temperature overnight. The reaction mixture is poured into water and the pH value thereof is adjusted to pH 12-14 by adding potassium carbonate. The mixture is extracted with chloroform, dried with sodium carbonate and then purified by silica gel column chromatography (solvent; n-hexane:ethyl acetate=1:1). The resultant is recrystallized from n-hexane/ethanol to give 1-{1-[4-(N-methylamino)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (1.2 g), as white powder, m.p. 184°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436254 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-3335bc8c187e439797f88b04ea94ffbc |
| Source note | uspto-grants-1995_07 |