HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301087Generated: November 1, 2026
1,1'-Carbonyldiimidazole → 2-t-Butoxycarbonyl-9-dimethylcarbamoylmethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole
https://huagongshe.com/reaction/2301087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-t-butoxycarbonyl-9-carboxymethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole | HCID 18377359 | — |
| Reactant | Dimethylamine tetrahydrofuran | HCID 22320367 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-t-Butoxycarbonyl-9-dimethylcarbamoylmethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole | HCID 11810445 | 96% |
Reaction Steps
The 2-t-butoxycarbonyl-9-carboxymethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole (1.65 g, 5.0 mmol) obtained in the above step (1) was dissolved in methylene chloride (30 ml), and the solution was mixed with carbonyldiimidazole (0.81 g, 5.0 mmol), stirred at room temperature for 30 minutes, mixed with 2 M dimethylamine-THF solution (3 ml, 6.0 mmol) and further subjected to 1 hour of the reaction. The reaction solution was concentrated, the resulting residue was dissolved in ethyl acetate (50 ml), washed with water and dried with anhydrous sodium sulfate, and then the solvent was removed by evaporation under a reduced pressure. By adding diisopropyl ether (30 ml) to the resulting residue, 1.71 g of the thus precipitated title compound (4.8 mmol, 96% in yield) was obtained as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498251B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-8fa8418439fe46c0ba44926bfb678d13 |
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| Source note | uspto-grants-2002_12 |
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