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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274771Generated: November 4, 2026

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

https://huagongshe.com/reaction/2274771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
Reactant6-fluoro-1-(phenylsulfonyl)-3-(1H-pyrazol-4-yl)-1H-indoleHCID 118060134—
Producttert-butyl 3-(4-(6-fluoro-1-(phenylsulfonyl)-1H-indol-3-yl)-1H-pyrazol-1-yl)azetidine-1-carboxylateHCID 118060252100.7%

Reaction Steps

Following the general method as outlined in Intermediate 16, starting from 6-fluoro-1-(phenylsulfonyl)-3-(1H-pyrazol-4-yl)-1H-indole (Intermediate 5; 812 mg; 2.38 mmol) and tert-butyl 3-iodoazetidine-1-carboxylate (674 mg; 2.38 mmol), 1.19 g (100%) of the title compound was obtained as a yellow solid, which was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126984B2
Source datasetuspto-grants-2015_09
ORD IDord-5b2cc1fe90c04f8fa0a6c63c7afd8eac
Source noteuspto-grants-2015_09