Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432699Generated: November 3, 2026

Methanesulfonic Acid → 2,6-Dimethyl-3-[3-methyl-5-(6-methyl-2-pyridinyl)thiophen-2-yl]-8-pentan-3-ylimidazo[1,2-b]pyridazine;methanesulfonic acid

https://huagongshe.com/reaction/1432699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant8-(1-Ethyl-propyl)-2,6-dimethyl-3-(3-methyl-5-pyridin-2-yl-thiophen-2-yl)-imidazo[1,2-b]pyridazineHCID 57932957—
SolventMethanolHCID 887—
Product2,6-Dimethyl-3-[3-methyl-5-(6-methyl-2-pyridinyl)thiophen-2-yl]-8-pentan-3-ylimidazo[1,2-b]pyridazine;methanesulfonic acidHCID 86620097200%

Reaction Steps

To a solution of 8-(1-ethyl-propyl)-2,6-dimethyl-3-(3-methyl-5-pyridin-2-yl-thiophen-2-yl)-imidazo[1,2-b]pyridazine (0.55 g, 1.36 mmol) and MeOH (6 mL) is added methane sulfonic acid (0.088 mL, 1.36 mmol). After one hour the solution is concentrated and the solution is treated with Darco-60® for 1 hour, filtered and concentrated to furnish the title compound (0.68 g, 1.36 mmol, >99%). 1H NMR (CDCl3: CD3OD 95:5) δ 0.85 (t, J=7.4 Hz, 6H), 1.67-1.91 (m, 4H), 1.96 (s, 3H), 1.97 (s, 3H), 2.20 (s, 3H), 2.61 (s, 3H), 2.90 (s, 3H), 3.17-3.29 (m, 1H), 7.33 (s, 1H), 7.64 (d, J=7.4 Hz, 1H), 7.89 (d, J=7.9 Hz, 1H), 8.18 (s, 1H), 8.34 (t, J=7.9 Hz, 1H), 9.95 (bs, 1H). LC/MS (m/z): calcd. for C25H32N4O2S2 (M+H)+: 405.6; found: 405.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612067B2
Source datasetuspto-grants-2009_11
ORD IDord-1b9887269b9945439adb52fabfd031da
Source noteuspto-grants-2009_11