HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Aminocarbonylamino-6-(1-hydroxyethyl)indole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Acetyl-2-aminocarbonylaminoindole-3-carboxamide | HCID 59189775 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Aminocarbonylamino-6-(1-hydroxyethyl)indole-3-carboxamide | HCID 59189886 | 22% |
Reaction Steps
Sodium borohydride (10 mg, 0.26 mmol) was added to a solution of 6-acetyl-2-aminocarbonylaminoindole-3-carboxamide (Compound 14-1,14 mg, 0.054 mmol) in anhydrous tetrahydrofuran (2 mL) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. Water (5 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (20 mL). The organic layer was washed with brine (5 mL), and dried over anhydrous magnesium sulfate. After the solvent was evaporated under reduced pressure, the resultant solid was washed with diethyl ether (2 mL) and dried under reduced pressure to give the title compound (3 mg) as a colorless solid (yield 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193237B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-c3ede20c1faf4393a8be07f577c14b7f |
| Source note | uspto-grants-2012_06 |