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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518248Generated: November 1, 2026

Diisopropylethylamine → HCID 86677060, compound

https://huagongshe.com/reaction/518248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
Reactant(S)-3-(1-aminoethyl)-8-chloro-2-phenylisoquinolin-1(2H)-oneHCID 66607319—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86677060HCID 86677060—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2,4-dichloro-5-nitropyrimidine (250 mg, 1.29 mmol, 1.15 eq.) in THF (2 mL) was chilled in a −78° C. bath. To this solution was slowly added over 40 mins a mixture of compound 1 (335 mg, 1.12 mmol, 1.0 eq.) and DIEA (450 μL, 2.58 mmol, 2.3 eq.) in THF (4 mL). After addition was complete, the reaction was stirred at −78° C. during 30-40 mins, then allowed to warm slowly to 15° C. over 1 h. The reaction mixture was diluted with DCM (40 mL), washed with water and brine (15 mL each), dried over Na2SO4, and concentrated. This residue was purified by flash chromatography eluting with 300 mL each 10/20/30/40% EtOAc/hexanes to give (S)-8-chloro-3-(1-(2-chloro-5-nitropyrimidin-4-ylamino)ethyl)-2-phenylisoquinolin-1(2H)-one 75. ESI-MS m/z: 456.15 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115141B2
Source datasetuspto-grants-2015_08
ORD IDord-3ece8f00e3e14b1e8281c487d7cd8627
Source noteuspto-grants-2015_08