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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709953Generated: November 1, 2026

Diisopropylethylamine → HCID 86662867, compound

https://huagongshe.com/reaction/709953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-iodopyrimidineHCID 263438—
ReactantHCID 66608768HCID 66608768—
Solvent1-ButanolHCID 263—
ProductHCID 86662867HCID 86662867—

Reaction Conditions

Temperature100 °C

Reaction Steps

(S)-3-(1-Aminoethyl)-8-(1-methyl-1H-pyrazol-4-yl)-2-phenylisoquinolin-1(2H)-one (63) (570 mg, 1.66 mmol), 2,4-dichloro-5-iodopyrimidine (455 mg, 1.66 mmol) and DIEA (0.27 mL, 1.66 mmol) were dissolved in n-butanol (12 mL) in a sealed tube, and the resulting mixture was stirred at 100° C. for 16 h. The mixture was allowed to cool to RT, quenched with water and extracted with ethyl acetate (150 mL×2). The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to afford the product (S)-3-(1-((2-chloro-5-iodopyrimidin-4-yl)amino)ethyl)-8-(1-methyl-1H-pyrazol-4-yl)-2-phenylisoquinolin-1(2H)-one (64) as an oil. The product obtained was used in the next step without purification. ESI-MS m/z: 583.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181221B2
Source datasetuspto-grants-2015_11
ORD IDord-bb048268457049a392ebba1d520c34b1
Source noteuspto-grants-2015_11