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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098448Generated: October 31, 2026

1,2-Dichloroethane → N-((1S)-1-{[(1S,4S)-5-(1H-indol-2-ylcarbonyl)-2,5-diazabicyclo[2.2.1]hept-2-yl]carbonyl}-2,2-dimethylpropyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/2098448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantIndole-2-carboxylic acidHCID 72899—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-{(1S)-1-[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-ylcarbonyl]-2,2-dimethylpropyl}-1H-indole-2-carboxamideHCID 67072627—
SolventDichloromethaneHCID 6344—
ProductN-((1S)-1-{[(1S,4S)-5-(1H-indol-2-ylcarbonyl)-2,5-diazabicyclo[2.2.1]hept-2-yl]carbonyl}-2,2-dimethylpropyl)-1H-indole-2-carboxamideHCID 4459903137.8%

Reaction Steps

To a solution of N-{(1S)-1-[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-ylcarbonyl]-2,2-dimethylpropyl}-1H-indole-2-carboxamide (120 mg, 0.34 mmol) in CH2Cl2 (4 mL) was added 1H-indole-2-carboxylic acid (55 mg, 0.34 mmol), EDC (78 mg, 0.41 mmol), HOBt (9 mg, 0.07 mmol) and NMM (102 mg, 0.93 mmol). The reaction mixture was stirred at room temperature for 3 h. The reaction was diluted with CH2Cl2 (5 mL) and washed with sat. NaHCO3 (10 mL), 1N HCl (10 mL), sat. NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried over Na2SO4, filtered, and concentrated to yield the crude product. The material was purified by HPLC (YMC C18 5.0 uM 250*20 mm) and then recrystallized from water, dried by lyophilization to afford 64 mg of the title compound: LCMS (m/z): 498.4 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 0.98-1.16 (9H, m), 1.83-2.07 (3H, m), 3.52-3.96 (4H, m), 4.65-5.20 (3H, m), 6.62-6.98 (3H, m), 7.06-7.18 (2H, m), 7.21-7.45 (3H, m), 7.53-7.68 (2H, m), 9.42-9.73 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450484B2
Source datasetuspto-grants-2013_05
ORD IDord-4ac7a31024a845888783eee23874c31f
Source noteuspto-grants-2013_05