Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30413Generated: October 24, 2026

1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine → 4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/en/reaction/30413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
ReactantBEMP resinHCID 16216994—
Reactant4-[1-(4-chloro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 68530176—
ReactantHCID 178518865HCID 178518865—
SolventDimethylformamideHCID 6228—
Product4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 6853283651%

Reaction Steps

4-[4-Fluoro-1-(2-fluoro-phenyl)-1H-indazol-3-yloxy]-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 46) was prepared as described above for Intermediate 42 using Intermediate 45 (300 mg, 1.218 mmol), PS-BEMP resin (1.108 g) and 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 2) (374 mg, 1.34 mmol) in DMF (10 ml) to afford 265 mg (51%) of Intermediate 46 as a yellow oil. MS (M+1)=430.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423054B2
Source datasetuspto-grants-2008_09
ORD IDord-150fdb8a77df4999909115a7edd9ba62
Source noteuspto-grants-2008_09