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
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 | 1,1-Dimethylethyl (1S,4S)-5-(3-methyl-L-valyl)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate | HCID 58286413 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-Dimethylethyl (1S,4S)-5-[N-(1H-indol-2-ylcarbonyl)-3-methyl-L-valyl]-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate | HCID 67215111 | 97.9% |
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
| 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-d607aecd6b924a1aaf7cd0b7c782ed73 |
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| Source note | uspto-grants-2013_05 |
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