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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278885Generated: October 27, 2026

Diisopropylethylamine → 2-Dimethylamino-4-methyl-pentanoic acid [2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethyl]-amide

https://huagongshe.com/reaction/278885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant(2S)-2-(dimethylamino)-4-methylpentanoic acidHCID 11658330—
Reactant(S)-2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethylamineHCID 70090603—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Dimethylamino-4-methyl-pentanoic acid [2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethyl]-amideHCID 1871179355.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-2-Dimethylamino-4-methyl-pentanoic acid (55.3 mg, 0.347 mmol) was dissolved in dry DMF (3 mL) under nitrogen atmosphere and cooled to 0° C. in an ice-water bath. To this solution were added in succession N,N-diisopropylethylamine (0.180 mL, 1.04 mmol) and solid O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (132 mg, 0.347 mmol, Novabiochem, La Jolla, Calif.). The resulting reaction mixture was stirred at that temperature for 30 minutes, (S)-2-(4-benzyloxy-phenyl)-1-morpholin-4-ylmethyl-ethylamine (153 g, 0.347 mmol, Example 3, Step D) was then added. After an additional 60 minutes stirring at 0° C., the reaction mixture was mixed with 60 mL of diethyl ether, and the resulting mixture was successively washed with saturated aqueous NaHCO3 solution and brine and then dried over Na2SO4. The solution was concentrated in vacuo, an oil was obtained. The crude product was purified by chromatography (silica gel, 10% methanol in chloroform) to give the title compound as a white solid (90 mg, 55%); mp 113-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362174B1
Source datasetuspto-grants-2002_03
ORD IDord-4d0a204cee834681801341e99aaf1ba9
Source noteuspto-grants-2002_03