HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(1-n butyl-4-piperidyl)methyl] indole-3-carboxamide → Quinolizidin-2-ylmethyl 2,3-dihydrothiazolo[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 | 2,3-Dihydrothiazolo[3,2-a]indole-9-carboxylic acid | HCID 19599448 | — |
| Reactant | Quinolizidin-2-ylmethylamine | HCID 82413010 | — |
| Product | Quinolizidin-2-ylmethyl 2,3-dihydrothiazolo[3,2-a]indole-9-carboxamide | HCID 131721476 | — |
Reaction Steps
2,3-Dihydrothiazolo[3,2-a]indole-9-carboxylic acid (D15) 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-793029023fd6478abaa1666bc5c24443 |
| Source note | uspto-grants-1999_12 |