HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 5-(1-Methylethoxy)-6-nitro-2-(4-piperidinyl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67071138 | HCID 67071138 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(1-Methylethoxy)-6-nitro-2-(4-piperidinyl)-1H-isoindole-1,3(2H)-dione | HCID 67071097 | — |
Reaction Steps
To a solution of 4-(5-isopropoxy-6-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester generated in the previous step in 3 mL of DCM is added TFA (3 mL). The reaction mixture is stirred at room temperature for 1 h. After concentration, water (5 mL) is added to the crude reaction mixture, the resulting mixture is neutralized to pH=8 by adding NaHCO3, and the product is extracted with DCM. The organic extracts are dried over Na2SO4, filtered and concentrated in vacuo to give crude 5-isopropoxy-6-nitro-2-piperidin-4-yl-isoindole-1,3-dione, which is directly used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377921B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-6ce60b9a5b52418ebba1680123fa6233 |
| Source note | uspto-grants-2013_02 |