HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 1-Chloroformyl-6,7,8,9-tetrahydropyrido[1,2-a]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 6,7,8,9-Tetrahydropyrido[1,2-a]indole | HCID 10855942 | — |
| Reactant | Methyl 6,7,8,9-tetrahydropyrido[1,2-a]indole-2-carboxylate | HCID 19778130 | — |
| Product | 1-Chloroformyl-6,7,8,9-tetrahydropyrido[1,2-a]indole | HCID 19778099 | — |
Reaction Steps
The methyl ester of Formula III wherein Z is --N(R2)-- and R1 and R2 are together --(CH2)3 --, namely methyl 6,7,8,9-tetrahydropyrido[1,2-a]indole-2-carboxylate, is prepared by reacting 6,7,8,9-tetrahydropyrido[1,2-a]indole with phosgene to form 1-chloroformyl-6,7,8,9-tetrahydropyrido[1,2-a]indole and subsequently converting this product to the methyl ester. A more detailed description of this procedure is set forth in Example 1 of this application. The 6,7,8,9-tetrahydropyrido[1,2-a]indole may be prepared via an intramolecular Wittig reaction (M. D. Crenshaw and H. Zimmer, J. Heterocyclic Chem., (1984) 21, 623).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189041 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-003faa9db6db43e2af199169d5b84038 |
| Source note | uspto-grants-1993_02 |