HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 53330391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67294188 | HCID 67294188 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53330391 | HCID 53330391 | 4.5% |
Reaction Steps
Acetyl chloride (18.3 mg) was added to a mixture of 6-(4-(3-aminopropoxy)-3-(trifluoromethyl)phenyl)-1-methyl-1H-[1,2,3]triazolo[4,5-c]pyridine-4-carbonitrile (100 mg) and triethylamine (294 μl) in DCM (2 ml). The mixture was stirred at room temperature for 2 hours then diluted with water, the organic layer was separated, dried over magnesium sulphate, and solvent was removed under reduced pressure. The residue was purified by HPLC to give the expected product (4.4 mg). 1H NMR (CD3OD) δ: 8.56 (s, 1H), 8.38-8.45 (m, 2H), 7.33 (d, 1H), 4.45 (s, 3H), 4.23 (t, 2H), 3.40 (t, 2H), 2.05 (quin, 2H), 1.95 (s, 3H). MS m/z 419 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115126B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-32d1ed1e50a84483abfe60cbd0beb0bf |
| Source note | uspto-grants-2015_08 |