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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174645Generated: October 30, 2026

Diisopropylethylamine → HCID 68483185, compound

https://huagongshe.com/reaction/2174645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromonicotinic acidHCID 88707—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant4-[(4-Methylpiperidin-1-yl)methyl]anilineHCID 1084995—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68483185HCID 68483185—

Reaction Steps

DIEA (473 μL, 2.72 mmol) was added into a solution of 5-bromonicotinic acid (178 mg, 0.881 mmol), 4-((4-methylpiperidin-1-yl)methyl)benzenamine (150 mg, 0.734 mmol), BOP (487 mg, 1.10 mmol) in DMF (3 mL). The reaction mixture is stirred at rt under argon atmosphere overnight. The reaction mixture was diluted with 80 mL of AcOEt, and then washed with 1N NaOH aqueous solution three times. Organic phase was dried with anhydrous Na2SO4, and then evaporated to remove organic solvents. The obtained residue was further dried under high vacuum overnight to give crude product, which was used directly for the next step synthesis without further purification. MS (ESI+) m/z 388.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062023B2
Source datasetuspto-grants-2015_06
ORD IDord-e06d24bf1aee4e20b2bd1c9a4c8bc5d3
Source noteuspto-grants-2015_06