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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Indole-2-carboxylic acid | HCID 72899 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | N-{(1S)-1-[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-ylcarbonyl]-2,2-dimethylpropyl}-1H-indole-2-carboxamide | HCID 67072627 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 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 | HCID 44599031 | 37.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450484B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-4ac7a31024a845888783eee23874c31f |
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| Source note | uspto-grants-2013_05 |
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