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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707411Generated: October 30, 2026

Diisopropylethylamine → HCID 178481624, compound

https://huagongshe.com/reaction/707411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-6-fluorobenzothiazoleHCID 2049870—
ReactantHCID 178478930HCID 178478930—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 178481624HCID 17848162443.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(trans-3-aminocyclobutyl)-6-fluoro-1-methyl-1H-imidazo[4,5-b]pyridin-2(3H)-one hydrochloride (0.100 g, 0.367 mmol), 2-chloro-6-fluorobenzothiazole (0.083 g, 0.440 mmol), and N,N-diisopropylethylamine (0.255 mL, 1.467 mmol) were mixed in DMSO (0.5 mL) in a sealed tube. The reaction mixture was stirred at 120° C. for 5 h. The reaction mixture was cooled to room temperature, diluted with water, and extracted with EtOAc. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered, and concentrated. The resulting crude product was purified by silica gel column chromatography eluting with EtOAc in hexanes to yield the title compound (0.062 g, 0.160 mmol, 43.6% yield) as an off-white solid. M+1: 388.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.40-2.49 (m, 2 H) 3.25-3.34 (m, 2 H) 3.36 (s, 3 H) 4.50-4.59 (m, 1 H) 5.21 (quin, J=8.36 Hz, 1 H) 7.08 (td, J=9.10, 2.74 Hz, 1 H) 7.41 (dd, J=8.80, 4.89 Hz, 1 H) 7.62-7.71 (m, 2 H) 8.05 (t, J=2.25 Hz, 1 H) 8.57 (d, J=6.26 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174992B2
Source datasetuspto-grants-2015_11
ORD IDord-8f1328bc981f4dc5894010076544cbb2
Source noteuspto-grants-2015_11