HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofurfuryl alcohol → HCID 25003273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 25003272 | HCID 25003272 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 25003273 | HCID 25003273 | 37% |
Reaction Steps
Sodium borohydride (18 mg, 0.48 mmol) was added to a solution of 2-aminocarbonylamino-5-(3-chlorophenyl)-4-formylpyrrole-3-carboxamide (Compound No. 17-1, 50 mg, 0.16 mmol) in the mixed solvent (tetrahydrofuran methanol=2:1, 1.5 mL) and the mixture was stirred at room temperature for 4 hours. Saturated aqueous ammonium chloride solution (50 mL) was added to the reaction solution, extracted with ethyl acetate (50 mL). The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The obtained solid was washed with chloroform (15 mL) and dried under reduced pressure to give the target compound (19 mg) as an orange solid (Yield 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977371B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-8d8e384063eb4b13aecec554da2a1688 |
| Source note | uspto-grants-2011_07 |