HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709953Generated: November 1, 2026
Diisopropylethylamine → HCID 86662867, compound
https://huagongshe.com/reaction/709953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-5-iodopyrimidine | HCID 263438 | — |
| Reactant | HCID 66608768 | HCID 66608768 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86662867 | HCID 86662867 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181221B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-bb048268457049a392ebba1d520c34b1 |
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| Source note | uspto-grants-2015_11 |
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