HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 66611240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | HCID 66612055 | HCID 66612055 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66611240 | HCID 66611240 | — |
Reaction Steps
To a solution of 5-[(phenylmethyl)oxy]-4-{[(phenylmethyl)oxy]carbonyl}-2-(trifluoromethyl)benzoic acid (may be prepared as described in Description 55; 142 mg, 0.14 mmol) in N,N-dimethylformamide (4 ml) was added diisopropylethylamine (120 ul), piperidine (0.05 ml, 0.52 mmol), 1-hydroxy-7-azabenzotriazole (60 mg), and EDC (120 mg). The solution was stirred for 18 hours. Water (10 ml) and ethyl acetate (10 ml) were added and the organic layer was separated, washed with water (2×10 ml), dried (MgSO4) and the solvent removed in vacuo. The residue was purified by column chromatography (SiO2, 1:1 ethyl acetate/cyclohexane) to yield the title compound as a gum. 170 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365551B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-c0ab7dca911746d587d730a1059aa8c0 |
| Source note | uspto-grants-2016_06 |