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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619252Generated: November 2, 2026

Tetrahydrofuran → N-{4-[2-(4-cyclopropylpiperazin-1-yl)benzothiazol-6-yl]phenyl}-acetamide

https://huagongshe.com/reaction/1619252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Acetamidophenylboronic acidHCID 2734657—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
Reactant6-Bromo-2-(4-cyclopropylpiperazin-1-yl)benzothiazoleHCID 59588803—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
ProductN-{4-[2-(4-cyclopropylpiperazin-1-yl)benzothiazol-6-yl]phenyl}-acetamideHCID 237289347.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 6-bromo-2-(4-cyclopropylpiperazin-1-yl)benzothiazole (500 mg, 1.48 mmol) and 4-acetamidophenylboronic acid (319 mg, 1.78 mmol) in a 5:1 mixture of THF and H2O (20 mL) was added Pd2(dba)3 (240 mg, 0.148 mmol), followed by P(t-Bu)3BF4 (86 mg, 0.296 mmol) and K3PO4.H2O (1.97 g, 7.4 mmol). The mixture was heated at 60° C. for 3 h, filtered and the volatiles were evaporated. Water (5 mL) was added and the mixture was extracted with CH2Cl2 (3×20 mL). The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by the preparative HPLC to give 42 mg (7%) of N-{4-[2-(4-cyclopropylpiperazin-1-yl)benzothiazol-6-yl]phenyl}-acetamide as a trifluoroacetate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772285B2
Source datasetuspto-grants-2014_07
ORD IDord-004eeb9ecaf449119425dff3259cc876
Source noteuspto-grants-2014_07