HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 57562597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57562612 | HCID 57562612 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57562597 | HCID 57562597 | — |
Reaction Steps
To a mixture of 28 mg of 6-((1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-3-yl)amino)pyrazine-2-carboxylic acid and 1 ml of N,N-dimethylformamide was added 84 mg of N,N′-carbonyldiimidazole, followed by stirring at room temperature for 15 hours. Then, 200 μl of an aqueous solution of 20 mg of sodium borohydride was added thereto and the resulting mixture was stirred. Water was added to the reaction mixture, and then the mixture was extracted with ethyl acetate. The resulting ethyl acetate solution was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated. The residue was purified by a silica gel column chromatography (eluent: chloroform to chloroform/methanol=10/1) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101621B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1b8aa34fcb554336b6bd4efd683a2b24 |
| Source note | uspto-grants-2012_01 |