HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178483343, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | HCID 178427713 | HCID 178427713 | — |
| Reactant | HCID 178527302 | HCID 178527302 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178483343 | HCID 178483343 | 93% |
Reaction Steps
2-[3-(Phenylsulfonyl)-1H-indazol-7-yl]ethyl 4-methylbenzenesulfonate To a solution of 2-[3-(phenylsulfonyl)-1H-indazol-7-yl]ethanol (0.64 g, 2.12 mmol) in anhydrous dichloromethane (30 mL) at 0° C. was added pyridine (0.43 mL) and toluenesulfonyl chloride (0.475 g, 2.5 mmol). The solution was stirred for 12 hours at room temperature. The mixture was concentrated in vacuo and taken up in ethyl acetate (30 mL). The organic layer was washed with 2 M HCl, (2×25 mL), brine, dried (MgSO4), filtered and concentrated under reduced pressure. Silica gel chromatography (50% ethyl acetate/petroleum ether) gave the title compound as a white foam (0.9 g, 93%). Mp: 61-64° C. MS (ES−): 455 (M−H) Step 7
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723329B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-1793ee27c5d74e0fa7bf7c03f81c95e7 |
| Source note | uspto-grants-2010_05 |