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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042768Generated: November 2, 2026

Diisopropylethylamine → N-(8-methoxytetralin-2-yl)-N-propyl-2-(2,5-dimethylphenyl)acetamide

https://huagongshe.com/reaction/2042768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,5-Dimethylphenylacetic acidHCID 83615—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant8-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amineHCID 12741417—
SolventDimethylformamideHCID 6228—
ProductN-(8-methoxytetralin-2-yl)-N-propyl-2-(2,5-dimethylphenyl)acetamideHCID 67250560—

Reaction Steps

A mixture of 340 mg (2.1 mmol) 2,5-dimethylphenylacetic acid (A3-4: W═OH, Cy=2,5-dimethylphenyl) and 0.70 mL diisopropylethylamine (DIPEA) (4.24. mmol) in 10 mL of dry DMF was cooled in an ice-bath. After addition of 950 mg (2.5 mmol) O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) in 5.0 mL dry DMF a solution of 640 mg (2.9 mmol) of the free base of N-(8-methoxytetralin-2-yl)-N-propylamine (A2-1) in 8.0 mL dry DMF was added dropwise, the ice-bath was removed and the reaction mixture was stirred for 3 hrs at room temperature. The mixture was washed with a saturated solution of aqueous NaHCO3 for several times and the resulting aqueous layer was extracted with CH2Cl2. The organic layers were dried over MgSO4 and the solvent was evaporated in vacuo. Flash chromatography of the residue on silica gel with a mixture of hexane/ethyl acetate 60/10 gave the product N-(8-methoxytetralin-2-yl)-N-propyl-2-(2,5-dimethylphenyl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586603B2
Source datasetuspto-grants-2013_11
ORD IDord-84ecdd422f8f4603976a73b168904544
Source noteuspto-grants-2013_11