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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359785Generated: November 3, 2026

N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide → tert-Butyl ({6-[(benzofuran-2-ylmethyl)(pyridin-3-ylsulfonyl)aminomethyl]-pyridin-2-yl}tert-butoxycarbonylamino)acetate

https://huagongshe.com/reaction/2359785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamideHCID 66717376—
ReactantN-(Benzofuran-2-ylmethyl)pyridin-3-ylsulfonamideHCID 66717414—
ReactantTert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetateHCID 86651768—
Producttert-Butyl ({6-[(benzofuran-2-ylmethyl)(pyridin-3-ylsulfonyl)aminomethyl]-pyridin-2-yl}tert-butoxycarbonylamino)acetateHCID 8671652788%

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 (252 mg, 0.745 mmol) obtained in Reference Example 3-(b), and using N-(benzofuran-2-ylmethyl)pyridin-3-ylsulfonamide (215 mg, 0.747 mmol) obtained in Reference Example 10-(c) in place of N-[4-(thiazol-2-yl)benzyl]pyridin-3-ylsulfonamide to afford the title compound (397 mg) as a white foam. (Yield: 88%) Mass spectrum (FAB, m/z): 609 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685986B2
Source datasetuspto-grants-2014_04
ORD IDord-acc0782e1fb14420885420556b7e0ab6
Source noteuspto-grants-2014_04