HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67951153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Isothiazolo(5,4-b)pyridin-3(2H)-one, 4,6-dimethyl- | HCID 173760 | — |
| Reactant | HCID 67811489 | HCID 67811489 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67951153 | HCID 67951153 | 11% |
Reaction Steps
Pyridinothiazolone 4 (300 mg, 1.66 mmol) was treated with ethyl 4-(2-iodoacetyl)piperazine-1-carboxylate (541 mg, 1.66 mmol), Et3N (840 mg, 8.30 mmol) and Cs2CO3 (500 mg, 1.54 mmol) in anhydrous CH2Cl2 (25 mL) at room temperature for 24 h, and then washed with H2O. The organic layer was dried over MgSO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (EtOAc/hexane (1:1)) to give the title compound (68 mg, 11% yield) in addition to the main N-alkylation product 21 (YMU1, 60%). The purity of product 28 was 99.5% as shown by HPLC on an HC-C18 column (Agilent, 4.6×250 mm, 5 μM), tR=4.9 min (gradients of 40-90% aqueous CH3CN in 15 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278982B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-a7809249720042b0825a19f44a8b606d |
| Source note | uspto-grants-2016_03 |