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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432439Generated: October 29, 2026

Thiazole → HCID 178423925, compound

https://huagongshe.com/reaction/432439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
Reactant2-Bromo-4'-methylacetophenoneHCID 69272—
ReactantHCID 178437379HCID 178437379—
ProductHCID 178423925HCID 178423925—

Reaction Steps

The procedure for thiazole synthesis, described in the preparation of cis-N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-4-ethyl-1,3-thiazol-2-amine, was employed with the exception that 2-bromo-4′-methylacetophenone (0.118 g, 0.554 mmol) was used as the alkylating agent. Purification of the product by preparative HPLC (25 to 100% acetonitrile in 0.1 M aqueous ammonium acetate over 20 min at 21 mL/min using an 8μ Hypersil HS C18, 250×21 mm column, Rt 9.1-10.7 min) afforded cis-N2-(4-{4-amino-1-[4-(4-methylpiperazino)cyclohexyl]-1H-pyrazolo[3,4-d]pyrimidin-3-yl}phenyl)-4-(4-methylphenyl)-1,3-thiazol-2-amine as an off-white powder (0.022 g, 0.038 mmol); RP-HPLC (25 to 100% acetonitrile in 0.1 M aqueous ammonium acetate over 10 min at 1 mL/min using a 5μ Hypersil HS C18, 250×4.6 mm column) Rt 8.88 min; MS (MH)+ 580.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-7829992de52444508ce59a6349e4d5e6
Source noteuspto-grants-2003_12