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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162440Generated: October 29, 2026

3-(Methylthio)benzeneboronic acid → N-(6-(3-(Methylthio)phenyl)imidazo[1,2-b]pyridazin-2-yl)acetamide

https://huagongshe.com/reaction/1162440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Methylthio)benzeneboronic acidHCID 2734383—
ReactantN-(6-(3-(4-Methylphenylsulfonamido)phenyl)imidazo[1,2-b]pyridazin-2-yl)acetamideHCID 44124523—
ReactantN-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 59519510—
ProductN-(6-(3-(Methylthio)phenyl)imidazo[1,2-b]pyridazin-2-yl)acetamideHCID 44124751—

Reaction Steps

Following the procedure described for compound N-(6-(3-(4-methylphenylsulfonamido)phenyl)imidazo[1,2-b]pyridazin-2-yl)acetamide (Example 1), N-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamide (Example 1, Step 4) (0.075 g, 0.36 mmol) was reacted with 3-(methylthio)phenylboronic acid (0.11 g, 0.64 mmol, Alfa Aesar, Ward Hill, Mass.) to afford the title compound as a yellow solid. MS (ESI positive ion) m/z: 299 (M+1). 1H NMR (400 MHz, DMSO-d6): δ ppm 10.91 (s, 1H), 8.30 (s, 1H), 8.06 (d, J=9.6 Hz, 1H), 7.90 (s, 1H), 7.80-7.82 (m, 2H), 7.49 (t, J=7.8 Hz, 1H), 7.40-7.42 (m, 1H), 2.57 (s, 3H), 2.11 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820665B2
Source datasetuspto-grants-2010_10
ORD IDord-de02c8c0fddf4836bee51d9b5e5267cb
Source noteuspto-grants-2010_10