Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Metoclopramide | HCID 4168 | — |
| Reactant | 4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-methoxybenzamide | HCID 10378510 | — |
| Product | HCID 14372582 | HCID 14372582 | 89% |
Reaction Steps
The general procedure of Preparation 1A was repeated except that the 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxybenzamide utilized therein was replaced by 4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-methoxybenzamide (prepared according to U.K. Patent Specification 1,793,771). The solvent (DMF) was removed in vacuo, and the residue treated with water and methylene chloride saturated with carbon dioxide, concentrated, and the crude product isolated in 89% yield by extraction with ethanol. A sample was chromatographed on a silica gel column using methylene chloride (97), methanol (3), ammonia (0.3) solvent system. The appropriate fractions were combined and concentrated in vacuo. The residue was crystallized from methanol to give the title compound as a colorless solid, mp. 163°-165°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011992 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-5447ee2ae1194ef4b447c3ec9b75f254 |
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| Source note | uspto-grants-1991_04 |
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