HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 59536329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | 1-(4-(Trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline | HCID 16640696 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59536329 | HCID 59536329 | — |
Reaction Steps
A solution of 1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (0.5 g, 2 mmol) (Example 9, step 3) in dichloromethane (10 mL) was treated with pyridine (1.4 mL, 17 mmol), triethylamine (0.5 mL, 4 mmol), potassium cyanate (0.3 g, 3 mmol), glacial acetic acid (1.00 mL, 17 mmol) and the resulting suspension was stirred at RT for 12 h. The reaction mixture was concentrated to a gummy residue which was taken up in dichloromethane (75 mL), washed with brine (35 mL), dried over anhydrous sodium sulfate, removed dichloromethane, and dried under high vacuum to yield (4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide as a white solid. MS (ESI pos. ion) m/z: 321 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476297B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-0c45b91acaad4fb1b02d317faee990ac |
| Source note | uspto-grants-2013_07 |