HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 2742017, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86654171 | HCID 86654171 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 2742017 | HCID 2742017 | 98% |
Reaction Steps
50 mg (1 eq.) of 4-(3-thiophen-2-yl[1,2,4]oxadiazol-5-yl)-piperidinium hydrochloride and 77 μl (3 eq.) of diisopropylethylamine were dissolved in 1 ml of dichloromethane. 39 μl (1.2 eq.) of acetic anhydride were added dropwise and the reaction medium was stirred for 2 hours at room temperature. The reaction medium was evaporated and the residue was taken up in 15 ml of ethyl acetate. The organic phase was washed with aqueous 1N sodium hydroxide solution (3×30 ml), with aqueous 1N hydrochloric acid solution (3×30 ml) and with saturated aqueous NaCl solution (30 ml), dried over MgSO4 and concentrated under reduced pressure to give 41 mg (98%) of the expected compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338599B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-936d5ea45c3744f2a2cbbd86ce4607bb |
| Source note | uspto-grants-2012_12 |