HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Trifluoromethanesulfonic acid 7-trifluoromethoxyisoquinolin-3-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Trifluoromethanesulfonic acid 5-chloro-8-fluoroisoquinolin-3-yl ester | HCID 86633140 | — |
| Reactant | HCID 178515360 | HCID 178515360 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Trifluoromethanesulfonic acid 7-trifluoromethoxyisoquinolin-3-yl ester | HCID 86633143 | — |
Reaction Steps
By following the procedure for the preparation of trifluoromethanesulfonic acid 5-chloro-8-fluoroisoquinolin-3-yl ester, the title compound was prepared from 7-trifluoromethoxyisoquinolin-3-ol (0.98 g, 4.3 mmol), triflic anhydride (0.17 mL, 1.0 mmol), NEt3 (0.8 mL, 3.0 mmol) and CH2Cl2 (10 mL). 1H NMR (CDCl3, 300 MHz): δ=7.63 (s, 1H), 7.65 (d, J=6.0 Hz, 1H), 7.89 (s, 1H), 7.98 (d, J=9.0 Hz, 1H), 9.10 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178668B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-e997272bd81b42438d23977ca11733ec |
| Source note | uspto-grants-2012_05 |