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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186566Generated: November 2, 2026

2-Chlorobenzylamine → HCID 66546705, compound

https://huagongshe.com/reaction/1186566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzylamineHCID 66648—
ReactantHCID 68227155HCID 68227155—
ProductHCID 66546705HCID 66546705—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of [3-(2-methanesulfonyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-yl]-(2-morpholin-4-yl-ethyl)-amine (from Example 50 supra) (200 mg, 0.50 mmol) and 2-chlorobenzylamine (281 mg, 1.99 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 the crude product (110 mg). Then the crude product was purified by prep-HPLC. Several drops of concentrated HCl were added to the fractions with product. After sonicating for several minutes, solution was concentrated under reduced pressure to afford {3-[2-(2-chloro-benzylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyrazin-8-yl}-(2-morpholin-4-yl-ethyl)-amine; hydrochloride. (Yield 58 mg, 25.1%). 1H NMR (300 MHz, CD3OD): δ 8.72 (s, 1H), 8.51 (s, 1H), 8.35 (s, 1H), 7.59 (d, 1H, J=6.9 Hz), 7.46-7.28 (m, 5H), 4.75 (brs, 2H), 4.17 (brs, 2H), 3.93 (brs, 4H), 3.59-3.28 (m, 5H). LC-MS: [M+H]+ 466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-78fd91b7d5f94f6c91c817eda3d25fca
Source noteuspto-grants-2014_03