HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Chloro-1H-indole-2-carboxylic acid [2-(4-hydroxy-piperidin-1-yl)-2-oxo-ethyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | N-[(5-chloro-1H-indol-2-yl)carbonyl]glycine | HCID 11436686 | — |
| Reactant | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Chloro-1H-indole-2-carboxylic acid [2-(4-hydroxy-piperidin-1-yl)-2-oxo-ethyl]-amide | HCID 15521015 | — |
Reaction Steps
4-Hydroxypiperidine (0.83 mmol) and [(5-chloro-1H-indole-2-carbonyl)-amino]-acetic acid (0.8 mmol) were coupled according to procedure A (dimethylformamide- dichloromethane reaction solvent) with the following workup: the reaction mixture was stirred with ethyl acetate and aqueous 2N HCl, the resulting suspension filtered and the collected solid washed successively with aqueous 2N HCl, aqueous 2N NaOH, ether and dried : Yield 180 mg, 68%; TSPMS 336/338 (MH+, 100%);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06107329 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-aedf34d0714d453ab42df8659f1f123e |
| Source note | uspto-grants-2000_08 |