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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-t-butoxycarbonyl-9-carboxymethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indoleHCID 18377359—
ReactantDimethylamine tetrahydrofuranHCID 22320367—
SolventDichloromethaneHCID 6344—
Product2-t-Butoxycarbonyl-9-dimethylcarbamoylmethyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indoleHCID 1181044596%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498251B1
Source datasetuspto-grants-2002_12
ORD IDord-8fa8418439fe46c0ba44926bfb678d13
Source noteuspto-grants-2002_12