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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15269Generated: November 1, 2026

Diisopropylethylamine → 3-Cyclohexyl-N-[2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-2-(S)-hydroxy-propionamide

https://huagongshe.com/reaction/15269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1H-Indole-1-ethanamine, 5-fluoro-2,3-dihydro-HCID 21082249—
Reactant(2S)-2-cyclohexyl-2-hydroxypropanoic acidHCID 68481045—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-Cyclohexyl-N-[2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-2-(S)-hydroxy-propionamideHCID 6847951528%

Reaction Steps

To a stirring suspension of (S)-cyclohexyl lactic acid (558 mg, 3.42 mmol) in CH2Cl2 was added 2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethylamine (616 mg, 3.42 mmol), HATU (1.429 g, 3.76 mmol), and DIEA (1.79 mL, 10.3 mmol). The reaction mixture was stirred at room temperature for several hours until the starting material had disappeared by LCMS. Ethyl acetate (100 mL) was added and the solution was washed with 1M NaHSO4 (2×100 mL), sat'd aq NaHCO3 (2×100 mL) and brine (1×100 mL). The solvent was removed in vacuo and the crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford 320 mg of 3-Cyclohexyl-N-[2-(5-fluoro-2,3-dihydro-indol-1-yl)-ethyl]-2-(S)-hydroxy-propionamide as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732449B2
Source datasetuspto-grants-2010_06
ORD IDord-3963630d9c554d238c06beab53f216e6
Source noteuspto-grants-2010_06