HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178461007, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl 4-formylbenzoate | HCID 2751588 | — |
| Reactant | HCID 90391302 | HCID 90391302 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178461007 | HCID 178461007 | 49.2% |
Reaction Steps
To a solution of N3-(2-chloro-4′-(isopropylsulfonyl)-6-(trifluoromethyl)biphenyl-4-yl)-1H-1,2,4-triazole-3,5-diamine (135 mg, 294 μmol) in MeOH (3.5 ml) was added tert-butyl 4-formylbenzoate (85 mg, 412 μmol) followed by acetic acid (52.4 mg, 50 μl, 873 μmol). The reaction was stirred at room temperature for 15 minutes, 2-picoline borane complex (42.4 mg, 396 μmol) was added and the stirring was continued for 3 days. The reaction mixture was poured into 0.1N HCl solution (20 ml) and the resulting suspension was filtered to collect the solid. The crude material was purified by flash chromatography (silica gel, 24 g, 3% to 5% MeOH in DCM) to afford a white solid as desired product (94 mg, 49% yield). MS +m/z: 650 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428469B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-30f1e78c72894bf69793cffdcad818a4 |
| Source note | uspto-grants-2016_08 |