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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198295Generated: October 31, 2026

Formaldehyde → 6-chloro-2,3,4,9-tetrahydro-2-methyl-9-(2-(2-methylpyrimidin-5-yl)ethyl)-1H-pyrido[3,4-b]indole

https://huagongshe.com/reaction/2198295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
Reactant4,4-Diethoxy-N-methylbutan-1-amineHCID 13994547—
Reactant5-(2-Bromoethyl)-2-methylpyrimidineHCID 66911720—
Reactant2-(5-chloro-1-(2-(2-methylpyrimidin-5-yl)ethyl)-1H-indol-3-yl)-N-methylethanamineHCID 66911781—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product6-chloro-2,3,4,9-tetrahydro-2-methyl-9-(2-(2-methylpyrimidin-5-yl)ethyl)-1H-pyrido[3,4-b]indoleHCID 44242177—

Reaction Steps

The title compound is prepared by following General Methods 1, 3 and 4 using 4-chlorophenylhydrazine hydrochloride, 5-(2-bromoethyl)-2-methylpyrimidine, and triethylamine (General Method 1), 3,1-(4-chlorophenyl)-1-(2-(2-methylpyrimidin-5-yl)ethyl)hydrazine (Example 1) and 4,4-diethoxy-N-methylbutan-1-amine (General Method 3) and 2-(5-chloro-1-(2-(2-methylpyrimidin-5-yl)ethyl)-1H-indol-3-yl)-N-methylethanamine (Example 10), formaldehyde and TFA in acetonitrile (General Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338447B2
Source datasetuspto-grants-2012_12
ORD IDord-3299044a7de9434892120250d4b0e709
Source noteuspto-grants-2012_12