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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205624Generated: November 2, 2026

Diisopropylethylamine → HCID 118214760, compound

https://huagongshe.com/reaction/2205624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-4-chloro-6-methyl-5-pyrimidinecarbonitrileHCID 75412446—
ReactantHCID 118214761HCID 118214761—
CatalystAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
ProductHCID 118214760HCID 118214760—

Reaction Conditions

Temperature75 °C

Reaction Steps

To crude tert-butyl (S)-4-((5-(1-aminoethyl)-1-methyl-1H-pyrrolo[3,2-b]pyridin-6-yl)amino)piperidine-1-carboxylate was added HOAc (2 drops), followed by ACN (2 mL), 2-amino-4-chloro-6-methylpyrimidine-5-carbonitrile (0.083 g, 0.493 mmol), and DIPEA (0.344 mL, 1.970 mmol). The reaction mixture was stirred at 75° C. for 1 hour. LCMS showed the reaction was complete, though messy. The volatiles were removed by N2 flow. The crude title compound was used without further purification. ESI-MS m/z [M+H]+ calc'd for C26H35N9O2, 506. found 506.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371321B2
Source datasetuspto-grants-2016_06
ORD IDord-2437996c2afe498ea11bb6a6078700d4
Source noteuspto-grants-2016_06