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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359781Generated: November 2, 2026

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

https://huagongshe.com/reaction/2359781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(thiazol-2-yl)benzyl]pyridin-2-ylsulfonamideHCID 66717382—
ReactantTert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetateHCID 86651768—
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 (279 mg, 0.824 mmol) obtained in Reference Example 3-(b), and using N-[4-(thiazol-2-yl)benzyl]pyridin-2-ylsulfonamide (275 mg, 0.830 mmol) obtained in Reference Example 5 in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide to afford the title compound (496 mg) as a white foam. (Yield: 92%) Mass spectrum (FAB, m/z): 652 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685986B2
Source datasetuspto-grants-2014_04
ORD IDord-4d9e9aea894f4715a5da65de80acd7f1
Source noteuspto-grants-2014_04