Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098661Generated: November 2, 2026

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

https://huagongshe.com/reaction/1098661

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 (29F, 3.0 g, 11.27 mmol) in methylene chloride (50.00 mL, 780.0 mmol) at room temperature. was treated with pyridine (4.56 mL, 56.33 mmol) and methanesulfonyl chloride (1.31 mL) and stirred at room temperature for 16 hours. 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 using chromatography (SiO2, EtOAc/Hexanes) to provide tert-butyl 5-(chloromethyl)-6-fluoro-1H-indazole-1-carboxylate (24G, 1.9 g; Yield=59%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143305B2
Source datasetuspto-grants-2012_03
ORD IDord-571f9593b6994a0d9d14b55cacfe5b72
Source noteuspto-grants-2012_03