Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186542Generated: November 3, 2026

tert-butyl N-(2-amino-2-phenylethyl)carbamate → (4-{3-[2-(2-Tert-butoxycarbonylamino-1-phenyl-ethylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-ylamino}-cyclohexyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1186542

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(2-amino-2-phenylethyl)carbamateHCID 2771847—
ReactantHCID 68226572HCID 68226572—
Product(4-{3-[2-(2-Tert-butoxycarbonylamino-1-phenyl-ethylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-ylamino}-cyclohexyl)-carbamic acid tert-butyl esterHCID 68227159—

Reaction Conditions

Temperature140 °C

Reaction Steps

The mixture of {4-[3-(2-methanesulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-ylamino]-cyclohexyl}-carbamic acid tert-butyl ester (from Example 48 supra) (170 mg, 0.36 mmol) and (2-amino-2-phenyl-ethyl)-carbamic acid tert-butyl ester (from Example 51 supra) (341 mg, 1.44 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 30:1) to afford crude (4-{3-[2-(2-tert-butoxycarbonylamino-1-phenyl-ethylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-ylamino}-cyclohexyl)-carbamic acid tert-butyl ester. (Yield 100 mg). LC-MS: [M+H]+ 644.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-eb05b51df9724266842bef4632ad45bb
Source noteuspto-grants-2014_03