Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775934Generated: November 1, 2026

Formaldehyde → HCID 44242374, compound

https://huagongshe.com/reaction/1775934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl bromoacetateHCID 7748—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactantm-Chlorophenylhydrazine hydrochlorideHCID 75331—
ReactantN,3-Dimethyl-1-butanamineHCID 521020—
Reactant4,4-Diethoxy-N-methylbutan-1-amineHCID 13994547—
ReactantHCID 66911678HCID 66911678—
ReactantHCID 66911687HCID 66911687—
ReactantHCID 66911765HCID 66911765—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
SolventSodium HydroxideHCID 14798—
SolventHCID 66911674HCID 66911674—
ProductHCID 44242374HCID 44242374—

Reaction Steps

The title compound is prepared by following General Methods 1, 3, 4, 5 and 7 by using 3-chlorophenylhydrazine hydrochloride, ethyl bromoacetate, and triethylamine (General Method 1), ethyl 2-(1-(3-chlorophenyl)hydrazinyl)acetate and 4,4-diethoxy-N-methylbutan-1-amine (General Method 3), ethyl 2-(6-chloro-3-(2-(methylamino)ethyl)-1H-indol-1-yl)acetate, formaldehyde and TFA in acetonitrile (General Method 4), ethyl 2-(7-chloro-1,2,3,4-tetrahydro-2-methylpyrido[3,4-b]indol-9-yl)acetate and NaOH (General Method 5), and 2-(7-chloro-1,2,3,4-tetrahydro-2-methylpyrido[3,4-b]indol-9-yl)acetic acid, N,3-dimethylbutan-1-amine and EDCI (General Method 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260429B2
Source datasetuspto-grants-2016_02
ORD IDord-348776917b9748bba5d0e6c46234c6a0
Source noteuspto-grants-2016_02