HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 44176511, compound → 2-(4-Carbamoylbenzyl)-n-(1-(4-cyanobenzyl)piperidin-4-yl)-2,3,4,5-tetrahydro-1h-pyrido[4,3-b]indole-8-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 44176511 | HCID 44176511 | — |
| Solvent | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | 2-(4-Carbamoylbenzyl)-n-(1-(4-cyanobenzyl)piperidin-4-yl)-2,3,4,5-tetrahydro-1h-pyrido[4,3-b]indole-8-carboxamide | HCID 44176618 | 182.9% |
Reaction Steps
A solution of tert-butyl 4-(2-(4-carbamoylbenzyl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole-8-carboxamido)piperidine-1-carboxylate (28, 745 mg, 1.4 mmol) in 4 N HCl/dioxane (20.0 mL) was allowed to stir at room temperature for 2 h. The reaction mixture was then concentrated to give a tan solid which was triturated with ethyl ether to give 2-(4-carbamoylbenzyl)-N-(1-(4-cyanobenzyl)piperidin-4-yl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole-8-carboxamide as an off-white solid (700 mg, 99%); MS (ES) 432 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895578B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-7297542ee07446d3be865cebbb13e7aa |
| Source note | uspto-grants-2014_11 |