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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410818Generated: November 2, 2026

HCID 66606459, compound → HCID 66604922, compound

https://huagongshe.com/reaction/2410818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66606459HCID 66606459—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 66604922HCID 6660492242%

Reaction Steps

A mixture of 7-nitro-2-(3-(trifluoromethyl)phenyl)-5H-pyrido[3,2-b]indole-4-carboxamide (200 mg, 0.500 mmol) and Pd-C (200 mg, 0.188 mmol)in MeOH (5 mL) under a H2 balloon was stirred for 3 hr. Filtration followed by preparative HPLC (100×30 mm Luna C18 column, Solvent A=10% Methanol, 90% H2O, 0.1% TFA; Solvent B=90% Methanol, 10% H2O, 0.1% TFA, 10-60% B at 42 mL/min over 20 min) and SCX capture and release with 2 N NH3 in MeOH afforded 7-amino-2-(3-(trifluoromethyl)phenyl)-5H-pyrido[3,2-b]indole-4-carboxamide (80 mg, 0.21 mmol, 41% yield). MS (ESI) m/z 371.09 (M+H). 1H NMR (500 MHz, DMSO-d6) δ ppm 11.16 (1H, d, J=4.58 Hz), 8.58 (2H, br. s.), 8.51 (1H, br. s.), 8.25-8.37 (1H, m), 7.86-7.99 (1H, m), 7.75 (3H, d, J=6.10 Hz), 6.82 (1H, d, J=3.36 Hz), 6.48-6.67 (1H, m), 5.61 (2H, br. s.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815840B2
Source datasetuspto-grants-2014_08
ORD IDord-46ba383864bc4b9b8624c87671ae1058
Source noteuspto-grants-2014_08