HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Batanopride Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrabutylammonium | HCID 16028 | — |
| Reactant | 3-Chloro-2-butanone | HCID 20026 | — |
| Reactant | o-Desmethyl metoclopramide | HCID 9817332 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Batanopride Hydrochloride | HCID 59691 | — |
Reaction Steps
A solution of the tetra-n-butylammonium salt of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (0.53 g, 1.0 mmole) in acetonitrile (6 ml) was treated with 3-chloro-2-butanone (0.11 ml, 0.12 g, 1.1 mmole) and stirred at 20° for 16 hours. After removal of the acetonitrile at reduced pressure, the residue was treated with 10 ml water and extracted with ethyl acetate. The extracts were washed with dilute sodium carbonate, dried and concentrated to leave an oil which was converted to a monohydrochloride salt with 1.0 ml 1N hydrochloric acid. Crystallization of this salt from 2-propanol-ethyl acetate gave the title compound, mp. 176°-179°. This material was identical to that prepared in Example 7C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808624 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-74584300215748aeb7a7e44a92f7622b |
| Source note | uspto-grants-1989_02 |