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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886915Generated: November 2, 2026

Diisopropylethylamine → HCID 67332211, compound

https://huagongshe.com/reaction/1886915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-Methylphenyl)-1,3-benzoxazol-5-amineHCID 721879—
Reactant4,4,4-Trifluorobutanoic acidHCID 2777085—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 67332211HCID 673322118.5%

Reaction Steps

To 4,4,4-trifluorobutanoic acid (128 mg, 0.90 mmol) in dry dimethylformamide (5 mL) was added HATU (397 mg, 1.05 mmol) and diisopropylethylamine (494 μL, 2.85 mmol). The mixture was then stirred at room temperature for 10 min. 2-p-Tolylbenzo[d]oxazol-5-amine (200 mg, 0.95 mmol) was then added and the resulting mixture was stirred at room temperature for 16 h. Ethyl acetate was added and the organic layer was washed once with saturated aqueous Na2CO3, followed by another wash with brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting with ethyl acetate/hexanes 40:60 v/v to afford 26.7 mg (8%) of the title compound (LCMS RT=6.77 min, MH+ 348.9)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501713B2
Source datasetuspto-grants-2013_08
ORD IDord-628d39471450421c950891a15e498b00
Source noteuspto-grants-2013_08