HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 5-(4-Chlorophenyl)-4-cyclopropyl-2-({1-[2-(trifluoromethyl)benzyl]-1H-1,2,4-triazol-5-yl}sulfonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Reactant | 5-(4-Chlorophenyl)-4-cyclopropyl-2-(1H-1,2,4-triazol-5-ylsulfonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 69940562 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(4-Chlorophenyl)-4-cyclopropyl-2-({1-[2-(trifluoromethyl)benzyl]-1H-1,2,4-triazol-5-yl}sulfonyl)-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 53378950 | — |
Reaction Steps
37 mg (0.10 mmol) of the compound from Example 93A were dissolved in 3 ml of dichloromethane, and 21 μl (0.13 mmol) of N,N-diisopropylethylamine were added. 30 mg (0.13 mmol) of 2-(trifluoromethyl)benzyl bromide dissolved in 1 ml of dichloromethane were then added, and the mixture was stirred at RT for 48 h. For work-up, the mixture was concentrated under reduced pressure and the crude product was purified chromatographically [Method 19]. This gave 33 mg (63% of theory) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187466B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-79fd83f3f76f4b4d870996ae3fe8715b |
| Source note | uspto-grants-2015_11 |