Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 20287095 | HCID 20287095 | — |
| Reactant | HCID 20287113 | HCID 20287113 | — |
| Reactant | HCID 20287125 | HCID 20287125 | — |
| Product | HCID 20287106 | HCID 20287106 | — |
Reaction Steps
Following essentially the same procedure but substituting methyl 2-hydroxy-5-[1-hydroxy-2-[4-(4-methoxyphenyl)-1-piperazinyl]ethyl]benzoate hydrochloride and methyl 2-hydroxy-5-[1-hydroxy-2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]benzoate hydrochloride for the methyl 2-hydroxy-5-[1-hydroxy-2-[4-(2-methylphenyl)-1-piperazinyl]ethyl]benzoate hydrochloride above and using gaseous methylamine in lieu of ammonia results in the preparation of 2-hydroxy-5-[1-hydroxy-2-[4-(4-methoxyphenyl)-1-piperazinyl]ethyl]-N-methylbenzamide monohydrochloride hydrate, having a m.pt. of 188°-9° C. (dec.), and 2-hydroxy-5-[1-hydroxy-2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-methylbenzamide monohydrochloride monohydrate, having a m.pt. of 162°-5° C. (dec.), respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255575 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-b0f91077220e4616b059853b58ca3804 |
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| Source note | uspto-grants-1981_03 |
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