HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → HCID 16112858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 59198428 | HCID 59198428 | — |
| Reactant | HCID 178504318 | HCID 178504318 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16112858 | HCID 16112858 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of 1-chloro-7-(trifluoromethyl)-5H-pyrido[4,3-b]indole-4-carbonitrile in a 3:2 (v/v) mixture of EtOH and conc. NH4OH (0.06 M) was heated at 150° C. for 2 h in a stainless steel pressure vessel. After cooling at room temperature, an excess of KOSiMe3 was added and the mixture was heated at 150° C. for 18 h. The reaction mixture was extracted with EtOAc and H2O. After evaporation of the organic solvent the residue was purified by flash chromatography (10% MeOH in EtOAc) to provide the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518964B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-46efcea418d6483abbb236c942c1a0ec |
| Source note | uspto-grants-2013_08 |