HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(3,4,5-Trimethoxyphenyl)benzyl chloride → 4-[N-(4-butylphenyl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(3,4,5-Trimethoxyphenyl)benzyl chloride | HCID 12021158 | — |
| Reactant | 4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine | HCID 22557866 | — |
| Product | 4-[N-(4-butylphenyl)-N-[4-(3,4,5-trimethoxyphenyl)benzyl]amino]-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine dihydrochloride | HCID 22558002 | — |
Reaction Steps
4-(4-Butylanilino)-1-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]piperidine (147 mg) and 4-(3,4,5-trimethoxyphenyl)benzyl chloride (114 mg) were condensed in the same manner as described in Example 9. The title compound was obtained as yellow powder after converting a free base to a dihydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498169B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-ab706c5338ee44e8a267d8b6abd6a0cd |
| Source note | uspto-grants-2002_12 |