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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856985Generated: October 26, 2026

Water → HCID 21864589, compound

https://huagongshe.com/reaction/856985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2,2-Diethoxyethyl)dimethylamineHCID 77163—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-Chloro-5-[5-(3-chlorothiophen-2-yl)-[1,2,4]oxadiazol-3-yl]-phenylamineHCID 9995637—
SolventAcetic AcidHCID 176—
ProductHCID 21864589HCID 2186458920.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirring solution of 2-chloro-5-[5-(3-chlorothiophen-2-yl)-[1,2,4]oxadiazol-3-yl]-phenylamine (0.121 g, 0.386 mmol), (dimethylamino)acetaldehyde diethyl acetal (0.720 mL, 3.94 mmol), glacial acetic acid (24.0 mL) and water (0.100 mL, 5.55 mmol) was added sodium cyanoborohydride (0.140 g, 2.22 mmol). The solution was heated at 60° C. for 5 days and then the solution was stirred at room temperature until a precipitate formed. The suspension was filtered, the filter cake was washed with EtOAc (10 mL) and then the filtrate was concentrated by rotary evaporation. The residue was purified by flash column chromatography (silica gel, elution with EtOAc:hexanes, 1:3.5), gave 0.027 g (20%) of the title compound as a white solid. 1H NMR (CDCl3): 7.60 (d, 1H, J=5.2 Hz), 7.44–7.35 (m, 3H), 7.13 (d, 1H, J=5.2 Hz), 4.33 (br s, 1H), 3.37–3.28 (m, 2H), 1.36 (t, 3H, J=7.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144876B2
Source datasetuspto-grants-2006_12
ORD IDord-c8f0a8b3d1384f2db8b3eb3880e05108
Source noteuspto-grants-2006_12