HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid benzyl-methyl-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid | HCID 68534120 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid benzyl-methyl-amide | HCID 68682226 | — |
Reaction Steps
The title compound was synthesized in analogy to example 1, from 5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid 1:1 hydrochloride, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (commercially available), methylbenzylamine (commercially available) and N,N-diisopropylethylamine in N,N-dimethylformamide to give the desired product after purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile/water/formic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723325B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-5d05388e59c542aa84b3bbddf0b4329c |
| Source note | uspto-grants-2010_05 |