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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355455Generated: October 31, 2026

Diisopropylethylamine → N-(1,3-Thiazol-2-yl)pyridin-2-amine 21

https://huagongshe.com/reaction/1355455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 11161046HCID 11161046—
Reactant2-Hydroxy-1-(piperazin-1-yl)ethan-1-one hydrochlorideHCID 18506883—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-(1,3-Thiazol-2-yl)pyridin-2-amine 21HCID 5329334—

Reaction Steps

2-{[4-(Chloromethyl)pyridin-2-yl]amino}-1,3-thiazole-5-carbonitrile (180 mg, 0.72 mmole) and 1-glycoloylpiperazine hydrochloride (259 mg, 1.44 mmole) were combined in DMSO (2 mL). To this was added diisopropylethylamine (0.38 mL, 2.15 mmole) at RT. After 3 hr the mixture was diluted with H2O and extracted with EtOAc (3×g). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (gradient, 5-15% EtOH/EtOAc then 5-10% MeOH/CHCl3) gave the title compound as a pale yellow solid: 1H NMR (d6-DMSO) δ12.19 (s, 1H), 8.33 (d, 1H, J=5.1 Hz), 8.32 (s, 1H), 7.14 (s, 1H), 7.04 (d, 1H, J=5.2 Hz), 4.54 (t, 1H, J=5.6 Hz), 4.08 (d, 2H, J=5.6 Hz), 3.55 (s, 2H), 3.49 (s, 2H), 3.36 (s, 2H), 2.38 (s, 4H); MS [M+H]+=359.1285.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586423B2
Source datasetuspto-grants-2003_07
ORD IDord-3046120b786542d0bfadcc3b11645a04
Source noteuspto-grants-2003_07