Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203145Generated: October 31, 2026

Water → HCID 178502305, compound

https://huagongshe.com/reaction/2203145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-4-[5-(4-bromo-2-chloro-5-trifluoromethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl esterHCID 67494940—
ReactantHCID 178502303HCID 178502303—
CatalystHCID 178418807HCID 178418807—
SolventTolueneHCID 1140—
ProductHCID 178502305HCID 17850230531%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of [(S)-2-Methyl-1-((S)-4-methyl-2-{4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-imidazol-2-yl}-2,5-dihydro-pyrrole-1-carbonyl)-propyl]-carbamic acid methyl ester (100 mg, 0.20 mmol, Preparation 4) and (R)-4-[5-(4-bromo-2-chloro-5-trifluoromethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester (110 mg, 0.19 mmol) dissolved in toluene (1.18 mL) and water (0.43 mL) was added potassium carbonate (127 mg, 0.92 mmol). The reaction mixture was sparged under nitrogen for 15 min and Pd(dppf)Cl2 CH2Cl2 (13.55 mg, 0.017 mmol) was added and the reaction mixture was sparged with nitrogen and heated to 90° C. overnight, cooled to RT, diluted with EtOAc and washed with water and brine to produce a dark colored solid, which was purified by silica gel chromatography (12 g silica, EtOAc/hexanes 40 to 100%) to produce the title intermediate (51 mg, 31% yield) as a yellowish colored solid. (m/z): [M+H]+ calcd for C44H50ClF3N8O7 895.34 found 895.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365549B2
Source datasetuspto-grants-2016_06
ORD IDord-50df153cc9a64d94888f77a9b43c1a66
Source noteuspto-grants-2016_06