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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158758Generated: October 25, 2026

9-ethyl-2-(methylamino)-9H-pyrido[2,3-b]indole-3-carboxamide → tert-butyl{(1S)-2-[3-(aminocarbonyl)-2-(methylamino)-9H-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamate

https://huagongshe.com/reaction/1158758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-ethyl-2-(methylamino)-9H-pyrido[2,3-b]indole-3-carboxamideHCID 24900932—
Reactanttert-butyl {(1S)-2-[2-amino-3-(aminocarbonyl)-9h-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamateHCID 59513639—
Producttert-butyl{(1S)-2-[3-(aminocarbonyl)-2-(methylamino)-9H-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamateHCID 5951364589%

Reaction Steps

tert-butyl{(1S)-2-[2-amino-3-(aminocarbonyl)-9H-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamate (xvi-b, 20 mg, 0.052 mmol) was alkylated according to procedure detailed in the preparation of 48, to afford tert-butyl{(1S)-2-[3-(aminocarbonyl)-2-(methylamino)-9H-pyrido[2,3-b]indol-9-yl]-1-methylethyl}carbamate (xxxii-a, 20 mg, 89%). NH4OAc QC conditions. M+H=398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812018B2
Source datasetuspto-grants-2010_10
ORD IDord-02f9b21527d4454f9db4f3dcf002d877
Source noteuspto-grants-2010_10