HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 5,6,7,8-Tetrahydro-2-methylquinoline | HCID 12229420 | — |
| Reactant | Methyl-2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate | HCID 12278958 | — |
| Reactant | Methyl 5,6,7,8-tetrahydroquinoline-2-acetate | HCID 20358396 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Product | 2-Methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide | HCID 12278968 | 30% |
Reaction Steps
Reaction of 2-methyl-5,6,7,8-tetrahydroquinoline with phenyl lithium and carbon dioxide followed by esterification according to the general method described in Examples 1B and 6B gave an inseparable mixture of methyl-2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxylate and methyl 5,6,7,8-tetrahydroquinoline-2-acetate which was converted without purification to a mixture of 2-methyl-5,6,7,8-tetrahydroquinoline-8-carboxamide and 5,6,7,8-tetrahydroquinoline-2-acetamide by reaction with ammonia using the method described in Example 2. Fractional recrystallisation from diisopropyl ether gave the title compound as colourless needles m.p. 114° (overall yield 30%) (Found: C, 69.31, H, 7.45, N, 14.7, C11H14N2O requires: C, 69.45, H, 7.42; N, 14.72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031102 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-5cb3c1028d574efb9b4bd510b9e45976 |
| Source note | uspto-grants-1977_06 |