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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984851Generated: October 31, 2026

Methylamine → HCID 9813880, compound

https://huagongshe.com/reaction/984851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 22285039HCID 22285039—
SolventEthyl AcetateHCID 8857—
ProductHCID 9813880HCID 98138804%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-methyl-4-chlorobenzo(g)imidazo(4,5-c)quinoline (Preparation 19 in Example 11) (130 mg, 0.49 mmol) and MeNH2 (2.0M/THF, 1.5 mL, 2.92 mmol) was heated in a pressure tube at 80° C. for 18 hours. After the reaction mixture was cooled to RT, it was diluted with EtOAc (100 mL), washed with sat'd NaCO3 (50 mL), and brine. The organic layer was dried over MgSO4, filtered and evaporated in vacuo. The crude material was submitted to flash chromatography (5% MeOH/EtOAc) affording the title compound as a pale white solid (5.2 mg, 4%). 1H NMR (CDCl3): 8.44 (s, 1H), 8.35 (s, 1H), 7.94 (d, J=8.3, 1H), 7.90 (d, J=8.3, 1H), 7.72 (s, 1H), 7.46 (m, 1H), 7.40 (m, 1H), 5.95 (b, 1H), 4.28 (s, 3H), 3.31 (s, 3H). (ESI) m/z (M+H)+=263.14. Inhibition of IKK-1 activity was measured using the assay of Example 2, where the inhibitory potential of the compound of Example 16 resulted in an IC50 of 0.80 μM.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869956B2
Source datasetuspto-grants-2005_03
ORD IDord-ca5a513ca78845a0bcdadc5a66158457
Source noteuspto-grants-2005_03