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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879599Generated: October 29, 2026

1-Tert-butylpiperazine → (S)-methyl 2-tert-butoxy-2-(2-(2-(4-tert-butylpiperazin-1-yl)pyrimidin-4-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)acetate

https://huagongshe.com/reaction/879599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butylpiperazineHCID 3530572—
Reactant(S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyrimidin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetateHCID 86700414—
Solvent1,4-DioxaneHCID 31275—
Product(S)-methyl 2-tert-butoxy-2-(2-(2-(4-tert-butylpiperazin-1-yl)pyrimidin-4-yl)-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)acetateHCID 86700415—

Reaction Steps

A flask was charged with (S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyrimidin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate (40.0 mg, 0.077 mmol) and 1-tert-butylpiperazine (33.1 mg, 0.232 mmol). 1,4-Dioxane (1 mL) was added, and the reaction mixture was stirred at room temperature for 3 h. Upon completion of the reaction, the reaction mixture was filtered through Celite (ethyl acetate eluent), concentrated, and used without further purification. LCMS-ESI+ calc'd for C33H41ClN5O3S (M+H+): 622.3; Found: 622.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-cccb573762804016a5a1f2772804baf4
Source noteuspto-grants-2015_03