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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226118Generated: November 1, 2026

HCID 68858146, compound → HCID 57752607, compound

https://huagongshe.com/reaction/226118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68858146HCID 68858146—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57752607HCID 5775260789%

Reaction Steps

A solution of 3-(5-fluoro-3-methyl-benzo[b]thiophen-2-yl)-2,6-dimethyl-8-(1-propyl-but-1-enyl)-imidazo[1,2-b]pyridazine (23 mg, 0.06 mmol), MeOH (19 mL), and 10% Pd—C (69 mg) is hydrogenated at 30 psi at room temperature for 2 hours. The mixture is filtered through celite, washed with EtOAC and concentrated to dryness to give the title compound (20.5 mg, 89%) %). 1H NMR (CDCl3): δ 7.8 (dd, J=4.8, 8.5 Hz, 1H), 7.5 (dd, J=2.5, 9.7 Hz, 1H), 7.2 (m, 1H), 6.9 (s, 1H), 3.69 (s, 1H), 2.62 (s, 3H), 2.58 (s, 3H), 2.4 (m, 2H), 2.3 (s, 3H), 1.8 (m, 4H), 1.29 (m, 4H), 0.93 (t, J=7.1, 6H) ppm. Mass spectrum (m/e): 410 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557103B2
Source datasetuspto-grants-2009_07
ORD IDord-ddb619d7f4784d04a3985a6f6f96eb00
Source noteuspto-grants-2009_07