HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminocarbonylamino-6-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]indole-3-c arboxamide → 2-Aminocarbonylamino-6-[4-(2-aminoethyl)phenyl]indole-3-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminocarbonylamino-6-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]indole-3-c arboxamide | HCID 59189776 | — |
| Reactant | HCID 86639075 | HCID 86639075 | — |
| Product | 2-Aminocarbonylamino-6-[4-(2-aminoethyl)phenyl]indole-3-carboxamide hydrochloride | HCID 68553297 | — |
Reaction Steps
4 N Hydrogene chloride dioxane solution (15 mL) was added to 2-aminocarbonylamino-6-[4-(2-tert-butoxycarbonylaminoethyl)phenyl]indole-3-c arboxamide (Compound 7-33, 65 mg, 0.15 mmol) under ice-cooling, and the mixture was stirred at room temperature overnight. After the reaction mixture was concentrated under reduced pressure, the precipitated solid was washed with ethyl acetate (3 mL), and dried under reduced pressure to give the title compound (56 mg) quantitatively as a slightly yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193237B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-b9410f550eef47219f19216039a471cb |
| Source note | uspto-grants-2012_06 |