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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432566Generated: November 3, 2026

1,2-Dimethoxyethane → HCID 57933064, compound

https://huagongshe.com/reaction/1432566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2,4-dimethyl-1,3-thiazoleHCID 298628—
Reactant8-(1-Ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine-3-yl boronic acidHCID 68840929—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 57933064HCID 5793306458.4%

Reaction Steps

To a microwave pressure tube is added 0.340 g (1.30 mmol) of 8-(1-ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazine-3-yl boronic acid, 0.100 g (0.521 mmol) of 5-bromo-2,4-dimethylthiazole, 0.361 g (0.313 mmol) of Pd(PPh3)4, 0.650 mL (1.30 mmol) of 2 M aqueous Na2CO3, and 2 mL 7:3:2 DME:H2O:EtOH, and the mixture is heated at 160° C. for 40 min. Reaction is checked by MS which indicates product present. The reaction mixture is partitioned between 75 mL of ethyl acetate and 75 mL of water. The layers are separated and the aqueous is extracted 3×50 mL of ethyl acetate, dried (MgSO4), and concentrated under vacuum. The crude mixture is purified by chromatography using hexanes/ethyl acetate as a solvent system. The product containing fractions are combined to obtain 0.100 g of the product, 58% yield. MS, ES+=329.2 (M+1); 1H-NMR (DMSO-d6)=6.974 (s, 1H); 3.085-3.052 (m, 1H); 2.665 (s, 3H); 2.438 (s, 3H); 2.290 (s, 3H); 2.147 (s, 3H); 1.849-1.727 (m, 4H); 0.776-0.738 (m, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612067B2
Source datasetuspto-grants-2009_11
ORD IDord-86db2408fe66436ea402cc69a97b7ae4
Source noteuspto-grants-2009_11