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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274782Generated: November 1, 2026

Tert-butyl 3-((methanesulfonyloxy)methyl)azetidine-1-carboxylate → tert-butyl 3-((4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazol-1-yl)methyl)azetidine-1-carboxylate

https://huagongshe.com/reaction/2274782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-((methanesulfonyloxy)methyl)azetidine-1-carboxylateHCID 21959416—
Reactant6-fluoro-1-(phenylsulfonyl)-3-(1H-pyrazol-4-yl)-1H-indoleHCID 118060134—
Reactanttert-butyl 4-((4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazol-1-yl)methyl)piperidine-1-carboxylateHCID 118060320—
Producttert-butyl 3-((4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazol-1-yl)methyl)azetidine-1-carboxylateHCID 11806074576%

Reaction Steps

Following the general method as outlined in Intermediate 20, starting from 6-fluoro-1-(phenylsulfonyl)-3-(1H-pyrazol-4-yl)-1H-indole (Intermediate 5; 1.22 g; 3.56 mmol) and tert-butyl 3-(((methylsulfonyl)oxy)methyl)azetidine-1-carboxylate (1.40 g; 5.28 mmol), 1.37 g (76%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-b801877ca4b74b73bfa304c35134f3ae
Source noteuspto-grants-2015_09