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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162483Generated: October 28, 2026

HCID 44125257, compound → HCID 44125254, compound

https://huagongshe.com/reaction/1162483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 44125257HCID 44125257—
ReactantN-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-b]pyridazin-2-yl)acetamideHCID 57749440—
ReactantHCID 59519519HCID 59519519—
ProductHCID 44125254HCID 4412525426%

Reaction Steps

Following the procedure described for compound N-(6-(6-chloro-5-(4-(2-hydroxypropan-2-yl)phenylsulfonamido)pyridin-3-yl)imidazo[1,2-b]pyridazin-2-yl)acetamide (Example 35), N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-b]pyridazin-2-yl)acetamide (122 mg, 404 μmol) (Example 35, Step 3) was reacted with N-(5-bromo-2-chloropyridin-3-yl)morpholine-4-sulfonamide from Step 1 (120 mg, 336 μmol) to afford the title compound as a light green solid (40 mg, 26% yield). MS (ESI positive ion) m/z: 452 (M+1). 1H NMR (400 MHz, DMSO-d6): δ ppm 2.12 (s, 3H), 3.12-3.18 (m, 4H), 3.60-3.68 (m, 4H), 7.86 (d, J=9.39 Hz, 1H), 8.14 (d, J=9.39 Hz, 1H), 8.33 (s, 1H), 8.54 (d, J=2.15 Hz, 1H), 8.90 (s, 1H), 10.14 (s, 1H), 10.97 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820665B2
Source datasetuspto-grants-2010_10
ORD IDord-f71c3a93233845039c62049f3c3564ca
Source noteuspto-grants-2010_10