HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216630Generated: October 25, 2026
Water → 2-[(Aminocarbonyl)amino]-6-ethynylindole-3-carboxamide
https://huagongshe.com/reaction/216630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | TBAF tetrahydrofuran | HCID 11078149 | — |
| Reactant | 2-Aminocarbonylamino-6-triisopropylsilylethynylindole-3-carboxamide | HCID 59189882 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(Aminocarbonyl)amino]-6-ethynylindole-3-carboxamide | HCID 24989060 | 90.8% |
Reaction Steps
1.0 M Tetrabutylammonium fluoride tetrahydrofuran solution (15 mL, 15 mmol) was added to a solution of 2-aminocarbonylamino-6-triisopropylsilylethynylindole-3-carboxamide (Compound 9-15, 4.0 g, 10 mmol) in anhydrous tetrahydrofuran (180 mL), and the mixture was stirred at 75° C. for 2.5 hours. Water (180 mL) was added to the reaction mixture, and the whole was extracted with ethyl acetate (180 mL). The organic layer was washed with brine (180 mL), and dried over anhydrous magnesium sulfate. After the solvent was evaporated under reduced pressure, the resultant solid was washed with a solution mixture of ethanol and chloroform (ethanol/chloroform=1/3, 55 mL) and dried under reduced pressure to give the title compound (2.2 g) as a slightly brown solid (yield 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08193237B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-d66b68c6c1194befae0588c840fa9d43 |
|---|
| Source note | uspto-grants-2012_06 |
|---|