HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 42606679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 42605984 | HCID 42605984 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 42606679 | HCID 42606679 | 67% |
Reaction Steps
To a suspension of 1-[(3,4-dichlorophenyl)methyl]-N-(5-formyl-1,3-thiazol-2-yl)-5-methyl-1H-1,2,3-triazole-4-carboxamide (Example 5) (1.2 g, 30 mmol), in a mixture of DCM/MeOH, was added sodium borohydride (130 mg). The reaction was stirred at room temperature for 1 hour. After evaporation, the residue was poured in a mixture of water/concentrated HCl solution and extracted with ethyl acetate. A solid was formed and filtered. The filtrate was dried over sodium sulphate and evaporated in vacuo. The combined solids were recrystallised from acetonitrile to give the title compound as a yellow solid (0.8 g, 67%). HRMS calculated for C15H13Cl2N5O2S (M+H)+ 398.0245, found: 398.0205, Rt: 2.59 min. MP: 170.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207204B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-49df11d6d19943acb489c9e01845aa37 |
| Source note | uspto-grants-2012_06 |