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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914774Generated: November 2, 2026

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

https://huagongshe.com/reaction/1914774

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 rt. was treated with pyridine (4.56 mL, 56.33 mmol) and methanesulfonyl chloride (1.31 mL) and stirred at rt. for 16 hours. The reaction mixture was concentrated in vacuo and the resulting 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 yield 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 numberUS08614229B2
Source datasetuspto-grants-2013_12
ORD IDord-e705d0fd78254920862e98725b977d31
Source noteuspto-grants-2013_12