HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 57500366, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57500364 | HCID 57500364 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57500366 | HCID 57500366 | 84% |
Reaction Steps
0.46 g (3.30 mmol) of potassium carbonate dissolved in 4 ml of water is added to the suspension of 0.80 g (1.65 mmol) of methyl 5-[(1-{[3-(acetyloxy)benzoyl]-amino}-2-methylindolizin-3-yl)carbonyl]-2-aminobenzoate in 16 ml of methanol. The reaction medium is stirred at ambient temperature for 1 hour, it gradually becomes homogenized. It is diluted with ethyl acetate and acidified with a molar solution of hydrochloric acid. The two phases are separated. The organic phase is washed with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. The solid obtained is taken up in ethyl ether and then filtered and dried. 0.61 g (84%) of a greenish yellow powder is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120819B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-3fba2870b98c4fd285442264ffc9b98d |
| Source note | uspto-grants-2015_09 |