HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441692Generated: November 1, 2026
Trifluoroacetic acid → HCID 59164595, compound
https://huagongshe.com/reaction/1441692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylate | HCID 10353694 | — |
| Reactant | 2-Chloro-6-trifluoromethylbenzothiazole | HCID 11470419 | — |
| Reactant | HCID 59164596 | HCID 59164596 | — |
| Reactant | HCID 68406062 | HCID 68406062 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59164595 | HCID 59164595 | 35.8% |
Reaction Steps
1.1 g 4-{2-[[2-(4-Cyano-3-methyl-phenyl)-ethyl]-(6-trifluoromethyl-benzothiazol-2-yl)-amino]-ethyl}-piperidine-1-carboxylic acid tert-butyl ester [prepared according to the method described in Example 1 and 5 from 4-(2-Amino-ethyl)-2-methyl-benzonitrile trifluoro acetate, N-boc-piperidinyl-4-acetaldehyde and 2-Chloro-6-trifluoromethyl-benzothiazole] were dissolved in 50 ml dichloromethane. 5 ml trifluoroacetic acid were added and the reaction mixture was stirred at room temperature for one hour. 150 ml ethyl acetate were added and the mixture was washed three times with saturated NaHCO3 solution. The organic layer was dried over MgSO4 and then the solvent was removed in vacuo. The residue was purified by RP-HPLC to obtain 325 mg 2-Methyl-4-{2-[(2-piperidin-4-yl-ethyl)-(6-trifluoromethyl-benzothiazol-2-yl)-amino]-ethyl}-benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07655679B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-d22327a4dd2e4452884e5e6bcbc1c048 |
|---|
| Source note | uspto-grants-2010_02 |
|---|