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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098245Generated: November 1, 2026

Diisopropylethylamine → HCID 178522480, compound

https://huagongshe.com/reaction/2098245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acidHCID 2794637—
ReactantHCID 178419692HCID 178419692—
SolventDimethylformamideHCID 6228—
ProductHCID 178522480HCID 17852248098.4%

Reaction Steps

A mixture of 6-chloro-imidazo[1,2-b]pyridazine-2-carboxylic acid (2.5 g), HBTU (4.41 g) and DIEA (4.0 mL) in DMF (20 mL) were stirred at room temperature for 10 minutes. To this reaction mixture was added 5-(3-trifluoromethoxy-phenyl)-1H-benzoimidazol-2-ylamine hydrobromide salt (3.78 g), and the mixture was heated at 80° C. for 30 minutes. After cooling the reaction mixture to room temperature, an aqueous sodium bicarbonate solution (200 mL) was added, and the mixture was stirred for 30 minutes. The mixture was then filtered, washed with water, dried, and purified on an 80 g pre-packaged silica gel column with a gradient of 0 to 10% 2M ammonia-methanol in DCM. 4.7 g of 6-chloro-imidazo[1,2-b]pyridazine-2-carboxylic acid [5-(3-trifluoromethoxy-phenyl)-1H-benzoimidazol-2-yl]-amide was obtained. LCMS (m/z): 473.9. 1H NMR (400 MHz, DMSO-d6) δ 12.14 (2H, br. s.) 9.08 (1H, s) 8.35 (1H, d) 7.81 (1H, s) 7.73 (1H, d) 7.47-7.65 (5H, m) 7.34 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450354B2
Source datasetuspto-grants-2013_05
ORD IDord-d5a1dc306b6d4246bbb0587cdc710b59
Source noteuspto-grants-2013_05