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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755378Generated: November 4, 2026

Sodium Hydroxide → 3-(8-(6-(2,5-Dimethylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoic acid

https://huagongshe.com/reaction/1755378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-(8-(6-(2,5-dimethylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoateHCID 86682732—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(8-(6-(2,5-Dimethylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoic acidHCID 7152626359%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of methyl 3-(8-(6-(2,5-dimethylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoate (150 mg, 0.34 mmol) and NaOH (150 mg, 3.75 mmol) in 1,4-dioxane (5 mL) and water (5 mL) was stirred for 2 h at 40° C. Then the mixture was concentrated to 5 mL then adjusted to pH=2 with 2M HCl. The precipitate was filtered and the solid was washed with water (2 mL) and dichloromethane (3 mL) to give 3-(8-(6-(2,5-dimethylpyrrolidin-1-yl)pyridin-2-ylamino)imidazo[1,2-b]pyridazin-6-yl)benzoic acid (86 mg, 59%) as a yellow solid. 1H NMR (300 MHz, DMSO): δ 10.79 (s, 1H), 9.13 (s, 1H), 8.62 (s, 1H), 8.49 (s, 1H), 8.32-8.14 (m, 3H), 7.75 (t, 1H, J=7.8 Hz), 7.54 (t, 1H, J=8.1 Hz), 6.74 (d, 1H, J=7.8 Hz), 6.23 (d, 1H, J=8.7 Hz), 4.12 (s, 2H), 2.13-2.08 (m, 2H), 1.74-1.68 (m, 2H), 1.18 (s, 3H), 1.16 (s, 3H). LC-MS: [M+H]+, 429, tR=1.708 min, HPLC: 97.23% at 214 nm, 95.49% at 254 nm, tR=6.248 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169259B2
Source datasetuspto-grants-2015_10
ORD IDord-cf793c75c636464e83aee41cce9d0cf4
Source noteuspto-grants-2015_10