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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718641Generated: October 28, 2026

Water → HCID 178437526, compound

https://huagongshe.com/reaction/718641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant(E)-4-(3-(6-Chloropyridin-3-yl)-2-(2-(quinolin-2-yl)vinyl)imidazo[1,2-b]pyridazin-8-yl)morpholineHCID 117728799—
ReactantHCID 178527972HCID 178527972—
SolventDimethylacetamideHCID 31374—
ProductHCID 178437526HCID 178437526—

Reaction Conditions

Temperature140 °C

Reaction Steps

A solution of compound 49a (0.50 g, 1.1 mmol) in DMA (3 mL) was treated with 4H-1,2,4-triazole-3-thiol (0.16 g, 1.6 mmol) and potassium tert-butoxide (0.24 g, 2.1 mmol). The resulting mixture was stirred at 140° C. for 3 h, allowed to cool to rt and treated with water (10 mL). The solids obtained were collected by filtration and purified by RP Prep-HPLC. The title compound 22 was obtained as a yellow solid. 1H-NMR (300 MHz, DMSO-d6) δ (ppm): 14.65 (s, 1H), 8.86 (s, 1H), 8.74 (s, 1H), 8.31 (d, J=8.7 Hz, 1H), 8.13 (d, J=5.7 Hz, 1H), 8.08-8.05 (m, 1H), 7.99-7.92 (m, 3H), 7.81-7.70 (m, 3H), 7.58-7.52 (m, 1H), 7.36 (d, J=7.8 Hz, 1H), 6.44 (d, J=6.0 Hz, 1H), 4.15-4.05 (m, 4H), 3.85-3.75 (m, 4H). Mass Spectrum (LCMS, ESI pos.): Calcd. for C28H23N9OS: 534.2 (M+H). Found: 534.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-bc3839e1d7e947b98bcb015128269c11
Source noteuspto-grants-2015_11