HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzothiazole → HCID 59351220, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Reactant | HCID 59351239 | HCID 59351239 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59351220 | HCID 59351220 | — |
Reaction Steps
4-(3-(Tetrahydro-2H-pyran-3-yl)pyrazin-2-yloxy)aniline (0.082 g, 0.30 mmol) and 2-chlorobenzothiazole (0.039 mL, 0.30 mmol) were mixed in isopropyl alcohol (0.50 mL) in a microwave tube. The tube was sealed, and the reaction mixture was refluxed for 2.5 h. The reaction mixture was cooled to room temperature, diluted with sat. sodium bicarbonate, and extracted with EtOAc (2×). The combined organic layers were washed with sat. sodium chloride, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude product was purified by silica gel chromatography to give N-(4-(3-(tetrahydro-2H-pyran-3-yl)pyrazin-2-yloxy)phenyl)benzo[d]thiazol-2-amine. MS (ESI, pos. ion) m/z: 405.1 (M+1). IC50 (uM) +++++.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247418B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-f18f92f458b24b348320c2f6075f8900 |
| Source note | uspto-grants-2012_08 |