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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098446Generated: October 31, 2026

1,2-Dichloroethane → 1,1-Dimethylethyl (1S,4S)-5-[N-(1H-indol-2-ylcarbonyl)-3-methyl-L-valyl]-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate

https://huagongshe.com/reaction/2098446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantIndole-2-carboxylic acidHCID 72899—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,1-Dimethylethyl (1S,4S)-5-(3-methyl-L-valyl)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylateHCID 58286413—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethylethyl (1S,4S)-5-[N-(1H-indol-2-ylcarbonyl)-3-methyl-L-valyl]-2,5-diazabicyclo[2.2.1]heptane-2-carboxylateHCID 6721511197.9%

Reaction Steps

To a solution of 1H-indole-2-carboxylic acid (14.6 g, 91 mmol) in CH2Cl2 (300 mL) was added 1,1-dimethylethyl (1S,4S)-5-(3-methyl-L-valyl)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (28.1 g, 91 mmol), EDC (20.9 g, 109 mmol), HOBt (2.45 g, 18 mmol), and NMM (25.2 g, 249 mmol). The reaction mixture was stirred at room temperature for 18 h. The reaction was diluted with CH2Cl2 and washed with sat. NaHCO3 (150 mL), 1N HCl (150 mL), sat. NaHCO3 (150 mL) and brine (200 mL). The organic layer was dried over Na2SO4, filtered, and concentrated to give the crude product which was purified by column chromatography (petroleum ether/ethyl acetate, 2:1). Concentration of the desired fractions afforded the title compound (40.5 g) as a yellow solid. LCMS (m/z): 455.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450484B2
Source datasetuspto-grants-2013_05
ORD IDord-d607aecd6b924a1aaf7cd0b7c782ed73
Source noteuspto-grants-2013_05