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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971022Generated: October 27, 2026

1-Cyclopropylethanamine → 1-[(1-Cyclopropylethyl)amino]-8-fluoro-5H-pyrido[4,3-b]indole-4-carbonitrile

https://huagongshe.com/reaction/1971022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-CyclopropylethanamineHCID 519239—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant1-chloro-8-fluoro-5H-pyrido[4,3-b]indole-4-carbonitrileHCID 59198492—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product1-[(1-Cyclopropylethyl)amino]-8-fluoro-5H-pyrido[4,3-b]indole-4-carbonitrileHCID 59543162—

Reaction Conditions

Temperature85 °C

Reaction Steps

1-Chloro-8-fluoro-5H-pyrido[4,3-b]indole-4-carbonitrile (400 mg, 1.63 mmol), 1-cyclopropylethanamine (594 mg, 4.89 mmol), Pd2(dba)3 (74.6 mg, 0.081 mmol), BINAP (152 mg, 0.24 mmol), and sodium tert-butoxide (782 mg, 8.14 mmol) were placed in a sealed tube. The mixture was evacuated and backfilled with argon three times. Fully degassed DME (8.1 ml) was added. The tube was sealed and the reaction was heated to 85° C. and stirred for 20 hrs. The reaction was cooled to ambient temperature, concentrated in vacuo, and directly purified via flash chromatography to afford the title compound. LRMS (APCI) calc'd for (C17H16FN4) [M+H]+, 295.1. found 295.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-bd8a8a6b38d14496af9496567f395c29
Source noteuspto-grants-2013_04