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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952232Generated: November 2, 2026

Pyridine → tert-butyl 5-(chloromethyl)-6-fluoro-1H-indazole-1-carboxylate

https://huagongshe.com/reaction/1952232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(1-Boc-6-fluoro-5-indazolyl)methanolHCID 59490881—
Producttert-butyl 5-(chloromethyl)-6-fluoro-1H-indazole-1-carboxylateHCID 5949089959.2%

Reaction Steps

A solution of tert-butyl 5-(hydroxymethyl)-6-fluoro-1H-indazole-1-carboxylate (22F, 3.0 g, 11.27 mmol) in methylene chloride (50.00 mL, 780.0 mmol) at rt. was treated with pyridine (4.56 mL, 56.33 mmol) and methanesulfonyl chloride (1.31 mL) and stirred at rt. for 16 h. The reaction mixture was concentrated in vacuo and the residue was dissolved in EtOAc (300 mL) washed with aq HCl (100 mL), brine (100 mL), dried (MgSO4), filtered, concentrated in vacuo, and purified by chromatography (SiO2, EtOAc/Hexanes) to yield tert-butyl 5-(chloromethyl)-6-fluoro-1H-indazole-1-carboxylate (22G, 1.9 g; Yield=59%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404845B2
Source datasetuspto-grants-2013_03
ORD IDord-a0ca1b37e6344f20ad5e517473174f85
Source noteuspto-grants-2013_03