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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624063Generated: October 25, 2026

Diisopropylethylamine → HCID 68283198, compound

https://huagongshe.com/reaction/624063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant2-(4-Amino-1H-pyrazol-1-yl)ethanolHCID 28492267—
Reactant5-(m-Tolyl)oxazole-4-carboxylic acidHCID 29923092—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 68283198HCID 68283198—

Reaction Steps

To a solution of 5-(m-tolyl)oxazole-4-carboxylic acid (5.50 g, 27.07 mmol) in DCM (80 mL), TBTU (13.04 g, 40.60 mmol) and DIPEA (13.90 mL, 81.20 mmol) was added. After stirring for 40 min at rt, 2-(4-amino-1H-pyrazol-1-yl)ethanol (3.47 g, 27.07 mmol) dissolved in DCM (10 mL) and DMF (4 mL) was added to the reaction mixture and stirred at rt for 1 h, then the reaction mixture was diluted with DCM and water, the org. layer was separated and the aq. layer extracted with DCM (1×). The combined org. layers were washed with brine, dried (MgSO4), filtered and the solvent was removed under reduced pressure. Purification by FC (DCM/MeOH, 95:5 to DCM/MeOH 9:1) yielded the tiltle compound as a white solid. LC-MS conditions A: tR=0.71 min, [M+H]+=313.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303023B2
Source datasetuspto-grants-2016_04
ORD IDord-0363448fe3a5466e9c68a1c6801143ad
Source noteuspto-grants-2016_04