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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896518Generated: October 27, 2026

Ammonium Hydroxide → 1-amino-5H-pyrido[4,3-b]indole-4-carboxamide

https://huagongshe.com/reaction/1896518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-chloro-5H-pyrido[4,3-b]indole-4-carboxamideHCID 59198457—
Product1-amino-5H-pyrido[4,3-b]indole-4-carboxamideHCID 23581927—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1-chloro-5H-pyrido[4,3-b]indole-4-carboxamide in conc. NH4OH (0.07 M) was heated in a microwave reactor at 160° C. for 1 h in a sealed tube. The reaction mixture was cooled to room temperature and partitioned between THF/EtOAc and saturated NaHCO3. After separation of the organic phase, the aqueous phase was extracted again with THF/EtOAc, and the combined organic phases were washed with brine, dried over Na2SO4 and filtered. After evaporation of the organic solvents, the residue was purified by flash chromatography (0-10% MeOH in EtOAc) to provide the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518964B2
Source datasetuspto-grants-2013_08
ORD IDord-49b2949afb5345aeb15da52b494fad4e
Source noteuspto-grants-2013_08