HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-(1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-methyl-1H-indole-6-carbonyl)piperazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-methyl-1H-indole-6-carboxylic acid | HCID 118666245 | — |
| Reactant | HCID 178517143 | HCID 178517143 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-methyl-1H-indole-6-carbonyl)piperazin-2-one | HCID 118671966 | — |
Reaction Steps
EDCxHCl (150 μmol) and N,N-diisopropylethylamine (380 μmol) were added to a solution of 1-(5-(2-fluorophenyl)pyrimidin-2-yl)-3-methyl-1H-indole-6-carboxylic acid (100 μmol) and hydroxybenzothiazol (30 μmol) in dichloromethane (4 mL) and the mixture was stirred for 15 min at room temperature. The appropriate amine (125 μmol) was added and the reaction mixture was stirred for 16 h at room temperature. The reaction was stopped by addition of saturated sodium hydrogen carbonate solution (2.5 mL) and the mixture was extracted with dichloromethane (3×3 mL). The solvent was removed under reduced pressure and the residue purified by preparative HPLC to furnish the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315490B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-fb80a17e48fc49179acbf3dfebfff757 |
| Source note | uspto-grants-2016_04 |