HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 59944552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 53781390 | HCID 53781390 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59944552 | HCID 59944552 | — |
Reaction Steps
To a stirred solution of pyrrolidine-1-carboxylic acid [3-(2-{benzyl-[4-(4-methanesulfonylaminophenyl)butyl]amino}ethyl)-2-(3,5-dimethylphenyl)-1H-indol-5-yl]-amide (16 mg in a mixture of 1 mL tetrahydrofuran and 3 mL methanol) was added 15 mg of 10% palladium hydroxide on carbon catalyst followed by acetic acid (0.015 mL of a 30% solution in water). The reaction flask was fitted with a hydrogen balloon, evacuated and recharged with hydrogen (3 times) and stirred at room temperature. After 25 minutes the reaction was flushed with nitrogen, filtered over diatomaceous earth and concentrated in vacuo. Purification by flash chromatography (methylene chloride:methanol:ammonium hydroxide, 90:8:1) gave the title compound (14 mg). m/e=602 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197975B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-3a0f95cdcb5945ff981ab8598f904fed |
| Source note | uspto-grants-2001_03 |