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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359794Generated: November 2, 2026

(4-(Pyridin-2-yl)phenyl)methanol → Tert-butyl[tert-butoxycarbonyl(6-{[4-(pyridin-2-yl)benzyl]-(pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-yl)amino]acetate

https://huagongshe.com/reaction/2359794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(Pyridin-2-yl)phenyl)methanolHCID 1515239—
ReactantN-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamideHCID 66717376—
ReactantTert-butyl (tert-butoxycarbonyl{6-[(pyridin-3-ylsulfonyl)aminomethyl]pyridin-2-yl}amino)acetateHCID 86651773—
ProductTert-butyl[tert-butoxycarbonyl(6-{[4-(pyridin-2-yl)benzyl]-(pyridin-3-ylsulfonyl)aminomethyl}pyridin-2-yl)amino]acetateHCID 86651780139.8%

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 (934 mg, 1.95 mmol) obtained in Reference Example 12-(d) in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide, and using 4-(pyridin-2-yl)benzyl alcohol (397 mg, 2.14 mmol) in place of tert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate to afford the title compound (1.76 g) (pure content 1.26 g) substantially quantitatively as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685986B2
Source datasetuspto-grants-2014_04
ORD IDord-bb15f2e483e0429da855871d33fcb9e3
Source noteuspto-grants-2014_04