HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23346088, compound → HCID 23346092, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23346088 | HCID 23346088 | — |
| Reactant | alpha,alpha-bis(trifluoromethyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-7-methanol | HCID 23346095 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 23346092 | HCID 23346092 | — |
Reaction Steps
By the method shown in Example 14, α,α-bis(trifluoromethyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-7-methanol is converted to α,α-bis(trifluoromethyl)-1-(1,3-dioxobutyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-7-methanol, m.p. 169°-171°, which is cyclized by heating in sulfuric acid (in this instance at 120° for 24 hours) to give 5,6,7,8-tetrahydro-10-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]-1-methyl-3H-azepino[3,2,1-ij]quinolin-3-one, m.p. 197°-198°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04218448 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-d5d4878da8524770bd94b593f855694b |
| Source note | uspto-grants-1980_08 |