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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241257Generated: October 25, 2026

N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide → Tert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate

https://huagongshe.com/reaction/241257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamideHCID 66717376—
Reactant4-(Pyridazin-4-yl)benzyl alcoholHCID 66717417—
ReactantTert-butyl (tert-butoxycarbonyl{6-[(pyridin-3-ylsulfonyl)aminomethyl]pyridin-2-yl}amino)acetateHCID 86651773—
ProductTert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetateHCID 86651768—

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-[(pyridin-3-ylsulfonyl)aminomethyl]pyridin-2-yl}amino)acetate (158 mg, 0.330 mmol) obtained in Reference Example 12-(d) in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide, and using 4-(pyridazin-4-yl)benzyl alcohol (60.2 mg, 0.323 mmol) obtained in Reference Example 13 in place of tert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate to afford the title compound (152 mg) as a white foam. (Yield: 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648097B2
Source datasetuspto-grants-2014_02
ORD IDord-5dce84a0f3cf437490e5f4b2fb6e336b
Source noteuspto-grants-2014_02