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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240094Generated: November 2, 2026

Pyridine → HCID 178483343, compound

https://huagongshe.com/reaction/2240094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantHCID 178427713HCID 178427713—
ReactantHCID 178527302HCID 178527302—
SolventDichloromethaneHCID 6344—
ProductHCID 178483343HCID 17848334393%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723329B2
Source datasetuspto-grants-2010_05
ORD IDord-1793ee27c5d74e0fa7bf7c03f81c95e7
Source noteuspto-grants-2010_05