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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099541Generated: October 31, 2026

Diisopropylethylamine → HCID 59773102, compound

https://huagongshe.com/reaction/2099541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Methyl-5-phenyl-3-furoic acidHCID 736516—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 53958485HCID 53958485—
SolventDimethylformamideHCID 6228—
ProductHCID 59773102HCID 5977310280.1%

Reaction Steps

Diisopropylethylamine (427 mg) was added to a stirred solution of 2-methyl-5-phenyl-furan-3-carboxylic acid (334 mg, 1.6 mmol) and ethyl-4-aminophenyl acetate (296 mg, 1.65 mmoles) in N,N-dimethylformamide (30 ml). 0-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (628 mg, 1.65 mmoles) was added and the solution was stirred at room temperature for 18 hours. The solvent was evaporated, the residue was dissolved in dichloromethane and washed with water, 10% aqueous sodium carbonate, 1M aqueous hydrochloric acid and finally dried (MgSO4). After evaporation of the solvent, the residue was triturated with cyclohexane and dried to afford (4-[(2-Methyl-5-phenyl-furan-3-carbonyl)-amino]-phenyl}-acetic acid ethyl ester (1)(466 mg) as a gum. LC/MS System D; Rt=10.64 mins, m/z (ES+)=364 (M+H for C22H21NO4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569602B2
Source datasetuspto-grants-2009_08
ORD IDord-9bd52e58561d464d9a9bf6e0f2420657
Source noteuspto-grants-2009_08