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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444630Generated: November 1, 2026

Indole → Methyl 14-cyclohexyl-5-[2-(dimethylamino)ethyl]-6-oxo-5,6,7,8-tetrahydroindolo[1,2-e][1,5]benzodiazocine-11-carboxylate

https://huagongshe.com/reaction/1444630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantSodium hydrideHCID 24758—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantMethyl 14-cyclohexyl-6-oxo-5,6,7,8-tetrahydroindolo[1,2-e][1,5]benzodiazocine-11-carboxylateHCID 68699073—
SolventDimethylformamideHCID 6228—
ProductMethyl 14-cyclohexyl-5-[2-(dimethylamino)ethyl]-6-oxo-5,6,7,8-tetrahydroindolo[1,2-e][1,5]benzodiazocine-11-carboxylateHCID 68699389—

Reaction Steps

NaH (1.4 eq, 60% dispersion in mineral oil) was added to a solution of methyl 14-cyclohexyl-6-oxo-5,6,7,8-tetrahydroindolo[1,2-e][1,5]benzodiazocine-11-carboxylate in DMF (0.1 M) and the solution allowed to stir at RT for 1 h. In the meantime, a 1:1 equimolar mixture of (2-chloroethyl)dimethylamine hydrochloride and NaH (60% dispersion in mineral oil) in solution in DMF (0.5 M) was prepared. After 30 mins, this mixture (2.5 eq of (2-chloroethyl)dimethylamine) was slowly added to the solution of indole anion and the mixture was stirred at RT overnight. DMF was removed in vacuo and the residue taken up in EtOAc. The organic phase was washed with H2O (twice) and then brine before being dried over Na2SO4, filtered and the solvent evaporated in vacuo. The crude compound was used in the next step without further purification; MS (ES+) m/z 474 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662809B2
Source datasetuspto-grants-2010_02
ORD IDord-9fa2f88fbfa24a32875848fa761db555
Source noteuspto-grants-2010_02