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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29095Generated: October 27, 2026

Sodium Chloride → Cyclopentyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine

https://huagongshe.com/reaction/29095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPerchloric AcidHCID 24247—
ReactantAminopyrazineHCID 78747—
ReactantCyclopentyl IsocyanideHCID 2734784—
Reactant5-(Phenylethynyl)thiophene-2-carbaldehydeHCID 2737140—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductCyclopentyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amineHCID 1171072647%

Reaction Steps

10 μl (0.022 mmol) of 20% aq. perchloric acid, a solution of 31.8 mg (0.15 mmol) of 5-phenylethynyl-thiophene-2-carbaldehyde in a mixture of MeOH and DCM (0.5 ml, 1:1 vol/vol) and a solution of 11.1 mg (0.115 mmol) of cyclopentyl isocyanide in MeOH (0.5 ml) were added in succession to a solution of 9.5 mg (0.1 mmol) of 2-aminopyrazine in MeOH (1 ml). The reaction solution was stirred at RT for 36 h and then combined with sat. aq. NaCl solution (3 ml) and stirred at RT for a further 45 min. The phases were separated and the aq. phase was extracted with DCM (2×3 ml). The collected organic phases were dried over MgSO4, filtered and evaporated under a vacuum. The group was purified by means of preparative HPLC, wherein 18 mg (0.047 mmol, 47%) of cyclopentyl-[2-(5-phenylethynyl-thiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-amine were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420056B2
Source datasetuspto-grants-2008_09
ORD IDord-d87eaf0a58864e0d80a02fd7c00519b7
Source noteuspto-grants-2008_09