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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186538Generated: November 3, 2026

HCID 68108044, compound → (2-{4-[8-(4-Methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2-thiophen-3-yl-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1186538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68108044HCID 68108044—
Reactant3-(2-Methanesulfonyl-pyrimidin-4-yl)-8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazineHCID 68226486—
Product(2-{4-[8-(4-Methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2-thiophen-3-yl-ethyl)-carbamic acid tert-butyl esterHCID 68226841—

Reaction Conditions

Temperature140 °C

Reaction Steps

The mixture of 3-(2-methanesulfonyl-pyrimidin-4-yl)-8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazine (from Example 46 supra) (200 mg, 0.536 mmol) and (2-amino-2-thiophen-3-yl-ethyl)-carbamic acid tert-butyl ester (from Example 74 supra) (520 mg, 2.14 mmol) was heated at 140° C., with stirring for 2 hours. The oil was purified by chromatography (silica gel, 10 g, 200-300 mesh, eluting with dichloromethane:methanol, 10:1 to 4:1) to afford crude (2-{4-[8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2-thiophen-3-yl-ethyl)-carbamic acid tert-butyl ester. (yield 150 mg). LC-MS: [M+H]+ 536.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-299ea1466d794e6699f1df33acf70b23
Source noteuspto-grants-2014_03