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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524243Generated: November 3, 2026

2-Thiazolamine, 5-bromo- → 5-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-1,3-thiazole-2-ylamine

https://huagongshe.com/reaction/1524243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiazolamine, 5-bromo-HCID 43600—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methyl-3-(trifluoroMethyl)pyrazole-5-boronic acidHCID 12056713—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
Product5-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-1,3-thiazole-2-ylamineHCID 866626831.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of (1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)boronic acid (290 mg, 1.5 mmol), 2-amino-5-bromothiazole (1 mmol), bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (A-Phos) (53 mg) and K3PO4 (212 mg, 1 mmol) in 2 ml ACN, 2 ml dioxane, 0.5 ml H2O was bubbled with argon before heated at 70° C. for 1 h. After cooling down to r.t., the reaction mixture was taken up in EA, washed with aq. NaHCO3 and brine, dried over Na2SO4, concentrated to dryness. Prep HPLC purification furnished 4.6 mg 5-[1-methyl-3-(trifluoromethyl)pyrazol-5-yl]-1,3-thiazole-2-ylamine (63) as light yellow solid (yield 1.9%; purity>95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079891B2
Source datasetuspto-grants-2015_07
ORD IDord-bd185c6d38b746c3a0f2d3eadb7a87c0
Source noteuspto-grants-2015_07