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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363344Generated: October 30, 2026

Diisopropylethylamine → HCID 86675758, compound

https://huagongshe.com/reaction/2363344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,2-DifluoroethanamineHCID 136274—
Reactant4-Chloro-2,5-difluorobenzoic acidHCID 2733274—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Solvent1,2-DichloroethaneHCID 11—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 86675758HCID 86675758—

Reaction Steps

A solution of 4-chloro-2,5-difluorobenzoic acid (1.28 g, 6.64 mmol), N,N-diisopropylethylamine (3.5 mL, 20 mmol), and N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (3.07 g, 8.07 mmol) in 1,2-dichloroethane (20 mL) was stirred for 10 min. at room temperature prior to the addition of a solution of 2,2-difluoroethanamine (538 mg, 6.64 mmol) in dichloroethane (2 mL). The resulting solution was stirred for 1 h. at room temperature. LCMS data indicated that the major reaction component was the desired product. The crude reaction mixture was concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with methanol in dichloromethane (0-10%) to afford the desired product. LCMS (M+H)+: m/z=256.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691807B2
Source datasetuspto-grants-2014_04
ORD IDord-9edbfee4724b47e5aa5846bb08a7355f
Source noteuspto-grants-2014_04