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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186502Generated: October 25, 2026

tert-butyl N-(2-amino-2-phenylethyl)carbamate → HCID 68226914, compound

https://huagongshe.com/reaction/1186502

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(2-amino-2-phenylethyl)carbamateHCID 2771847—
Reactant3-(2-Methanesulfonyl-pyrimidin-4-yl)-8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazineHCID 68226486—
ProductHCID 68226914HCID 6822691426%

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) (120 mg, 0.32 mmol) and (2-amino-2-phenyl-ethyl)-carbamic acid tert-butyl ester (from Example 51 supra) (305 mg, 1.29 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, 50:1 to 20:1) to afford crude (2-{4-[8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-2-phenyl-ethyl)-carbamic acid tert-butyl ester (Yield 44 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-bb81807842ff46f9bf042aa001cbfead
Source noteuspto-grants-2014_03