HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20291279, compound → HCID 23346102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20291279 | HCID 20291279 | — |
| Reactant | HCID 86737149 | HCID 86737149 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 23346102 | HCID 23346102 | — |
Reaction Steps
By the method of Example 7, α-(chlorodifluoromethyl)-α-(trifluoromethyl)-2,3-dihydro-1H-indole-5-methanol is converted to α-(chlorodifluoromethyl)-α-trifluoromethyl)-1-(1,3-dioxobutyl)-2,3-dihydro-1H-indole-5-methanol, m.p. 160°-164°, which is cyclized by heating in sulfuric acid to give 1,2-dihydro-8 [2-chloro-2,2-difluoro-1-hydroxy-1-(trifluoromethyl)ethyl]-6-methyl-4H-pyrrolo[3,-2,1-ij]quinolin-4-one, m.p. 294°-295°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04218448 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-98f626a047e54eb397f34338fc9169a5 |
| Source note | uspto-grants-1980_08 |