HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(1-n butyl-4-piperidyl)methyl] indole-3-carboxamide → Quinolizidin-2-ylmethyl thiazolo[3,2-a]indole-9-Carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(1-n butyl-4-piperidyl)methyl] indole-3-carboxamide | HCID 10591304 | — |
| Reactant | Thiazolo[3,2-a]indole-9-carboxylic acid | HCID 19599418 | — |
| Reactant | Quinolizidin-2-ylmethylamine | HCID 82413010 | — |
| Product | Quinolizidin-2-ylmethyl thiazolo[3,2-a]indole-9-Carboxamide | HCID 131720988 | — |
Reaction Steps
Thiazolo[3,2-a]indole-9-carboxylic acid (D16) is converted to its acid chloride and reacted with eq-quinolizidin-2-ylmethylamine (D12) using a procedure analogous to that described in Description 1b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998409 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-21e0f66f500c4571af86571c9c7a6fb5 |
| Source note | uspto-grants-1999_12 |