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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060916Generated: November 1, 2026

4-Amino-1-methylpiperidine → 5-Chloro-3,8-dimethyl-N-(1-methyl-4-piperidinyl)-9H-pyrido[2,3-b]indole-7-carboxamide

https://huagongshe.com/reaction/2060916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantHCID 57741423HCID 57741423—
Product5-Chloro-3,8-dimethyl-N-(1-methyl-4-piperidinyl)-9H-pyrido[2,3-b]indole-7-carboxamideHCID 16124308—

Reaction Steps

The title compound was synthesized from 5-chloro-3,8-dimethyl-9H-pyrido[2,3-b]indole-7-carboxylic acid and 1-methylpiperidin-4-amine using an analogous procedure to that described in the preparation of Compound 88. 1H NMR (400 MHz, DMSO-d6 with TFD) δ ppm 1.70-2.2 (m, 4H) 2.53 (br. s., 3H) 2.58 (s, 3H) 2.74-2.82 (m, 3H) 2.80-4.10 (m, 5H) 7.29 (s, 1H) 8.47 (s, 1H) 8.70 (s, 1H). [M+H] calc'd for C20H18N2O2S 371; found, 371.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278450B2
Source datasetuspto-grants-2012_10
ORD IDord-8707ab16ddc14f00b9222b5d9da8cd47
Source noteuspto-grants-2012_10