HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → Turofexorate isopropyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | HCID 57817588 | HCID 57817588 | — |
| Product | Turofexorate isopropyl | HCID 10026128 | — |
Reaction Steps
Ethyl 3-(3,4-difluorobenzoyl)-1,1-dimethyl-1,2,3,4,5,6-hexahydro-azepino[4,5-b]indole-5-carboxylate was saponified, converted to the corresponding isopropyl ester using CDl and isopropanol, and then oxidized as described previously in Step D of Example 63 to give the title compound; 1H-NMR (DMSO-d6): δ 10.83 (1H, s), 7.76 (1H, d), 7.71 (1H, app t), 7.64 (1H, s), 7.52-7.61 (2H, m), 7.40 (1H, m), 7.08 (1H, app t), 6.98 (1H, app t), 5.05 (1H, sept), 1.52 (6H, s), 1.18 (6H, d); MS(ESI): 439 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595311B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-67c0455f20694ec4965eaf9cecff2ca2 |
| Source note | uspto-grants-2009_09 |