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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620716Generated: November 1, 2026

Diisopropylethylamine → HCID 178456942, compound

https://huagongshe.com/reaction/1620716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-1-benzofuran-2-carboxylic acidHCID 937838—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178456897HCID 178456897—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178456942HCID 17845694221.5%

Reaction Steps

To a solution of (5Z)-4-(prop-2-yn-1-ylamino)-5-(piperidin-4-ylmethylidene)-1,3-thiazol-2(5H)-one dihydrochloride (200 mg) in DMF (3 mL) were added N-ethyl-N-(1-methylethyl)propan-2-amine (0.56 mL), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (283 mg), and 5-chlorobenzofuran-2-carboxylic acid (151 mg). The reaction mixture was stirred at room temperature overnight, water was added, the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/heptane to give the title compound (57 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-0a21847baa524bc9ad118097d55007de
Source noteuspto-grants-2014_07