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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245639Generated: October 29, 2026

Isopropylamine → HCID 178434361, compound

https://huagongshe.com/reaction/245639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
ReactantAcetonitrile--water (1/1)HCID 18373917—
Reactant5-chloro-7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-3-methyl-1H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-oneHCID 178434174—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178434361HCID 17843436128%

Reaction Steps

To a suspension of 148 mg (0.20 mmol) of the above 5-chloro-7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-3-methyl-1H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one in 5.92 mL of a mixture acetonitrile: H2O 4:1 (v/v) is added 51 μL (0.60 mmol) of isopropylamine. The reaction mixture is stirred for 6 hours at ambient temperature. Brine is then added to the mixture and the product is extracted with ethyl acetate (3 times). The regrouped organic phases are dried on Na2SO4, filtrated and evaporated. The purification of the residue by flash chromatography (SiO2, heptane/ethyl acetate 1:1) affords 30 mg (28%) of a white solid; LC/MS:540/542 (M+H)+, m.p.: 235-236° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658801B2
Source datasetuspto-grants-2014_02
ORD IDord-3e194bb5849e4ddca4ab72fa94daab57
Source noteuspto-grants-2014_02