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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359782Generated: October 27, 2026

4-fluoro-N-[4-(thiazol-2-yl)benzyl]benzenesulfonamide → N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide

https://huagongshe.com/reaction/2359782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-fluoro-N-[4-(thiazol-2-yl)benzyl]benzenesulfonamideHCID 54773958—
Reactant[Tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetateHCID 86651769—
ProductN-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamideHCID 66717376—

Reaction Steps

Reaction and post-treatment were carried out in the same manner as in Example 2-(a) except for using tert-butyl([tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate (101 mg, 0.298 mmol) obtained in Reference Example 3-(b), and using 4-fluoro-N-[4-(thiazol-2-yl)benzyl]benzenesulfonamide (105 mg, 0.301 mmol) obtained in Reference Example 6 in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide to afford the title compound (181 mg) as a white foam. (Yield: 91%) Mass spectrum (FAB, m/z): 669 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685986B2
Source datasetuspto-grants-2014_04
ORD IDord-a975e8b7a38b4439aa699dc51bfbcfb2
Source noteuspto-grants-2014_04