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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186530Generated: November 1, 2026

Hydrochloric Acid → HCID 66546144, compound

https://huagongshe.com/reaction/1186530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 68227032HCID 68227032—
SolventEthanolHCID 702—
ProductHCID 66546144HCID 66546144—

Reaction Steps

To a solution of crude (3-{4-[8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-ylamino}-3-thiophen-3-yl-propyl)-carbamic acid tert-butyl ester (400 mg, 0.182 mmol) in ethanol (3 mL) was added concentrated hydrochloric acid (3 mL) slowly. The reaction mixture was stirred at room temperature for 15 hours. The solvent was removed under reduced pressure and then the solid 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 N1-{4-[8-(4-methyl-piperazin-1-yl)-imidazo[1,2-a]pyrazin-3-yl]-pyrimidin-2-yl}-1-thiophen-3-yl-propane-1,3-diamine; hydrochloride. (Yield 27 mg, 14.9%). 1H NMR (300 MHz, CD3OD): δ 8.76 (s, 2H), 8.41 (brs, 1H), 7.68-7.52 (m, 4H), 7.32 (d, 1H, J=5.1 Hz), 5.55 (brs, 1H), 4.85 (brs, 2H), 3.75-3.72 (m, 4H), 3.40(brs, 2H), 3.18-3.15 (m, 2H), 3.00 (s, 3H), 2.44 (brs, 2H). LC-MS: [M+H]+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673905B2
Source datasetuspto-grants-2014_03
ORD IDord-54dcea19558d41b2b68705dce38fa82d
Source noteuspto-grants-2014_03