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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398496Generated: November 1, 2026

Piperidine → N-(2-amino-4-{6-[3-hydroxy-3-(1,3-thiazol-2-yl)but-1-yn-1-yl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyloxetane-3-carboxamide

https://huagongshe.com/reaction/1398496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-(Thiazol-2-yl)but-3-yn-2-olHCID 58221551—
ReactantN-[2-amino-4-(6-iodo-1H-indazol-1-yl)pyrimidin-5-yl]-3-methyloxetane-3-carboxamideHCID 68181899—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
ProductN-(2-amino-4-{6-[3-hydroxy-3-(1,3-thiazol-2-yl)but-1-yn-1-yl]-1H-indazol-1-yl}pyrimidin-5-yl)-3-methyloxetane-3-carboxamideHCID 60164065—

Reaction Steps

To a mixture of N-[2-amino-4-(6-iodo-1H-indazol-1-yl)pyrimidin-5-yl]-3-methyloxetane-3-carboxamide (76% purity, 20 mg, 0.034 mmol) and piperidine (0.1 mL) was added tetrakis(triphenylphosphine)palladium (7.8 mg, 0.007 mmol), copper(I) iodide (1.2 mg, 0.007 mmol) and 2-(1,3-thiazol-2-yl)but-3-yn-2-ol (I-1) (10.3 mg, 0.068 mmol). The reaction was purged with N2 and stirred at RT for 2 hr. Reaction mixture was concentrated in vacuo. Purification by flash chromatography (Isolute column, 100% DCM to 2% MeOH-DCM) followed by recrystallization (1:1 MeOH-EtOAc mixture) gave the title compound: 1H NMR (500 MHz, MeOD) δ 1.73 (3H, s), 1.98 (3H, s), 4.47 (2H, d, J=5.99 Hz), 5.01 (2H, d, J=6.15 Hz), 7.43 (1H, dd, J=8.28, 1.18 Hz), 7.57 (1H, d, J=3.31 Hz), 7.79 (1H, d, J=3.31 Hz), 7.83 (1H, d, J=8.35 Hz), 8.39 (1H, s), 8.82 (1H, s), 8.92 (1H, s); m/z=+476.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901313B2
Source datasetuspto-grants-2014_12
ORD IDord-0eddf92850f841a3b1d60f0a6e0c1421
Source noteuspto-grants-2014_12