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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776021Generated: October 30, 2026

Water → HCID 178466961, compound

https://huagongshe.com/reaction/1776021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-4-[5-(4-bromo-3-ethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl esterHCID 67495118—
ReactantHCID 178502353HCID 178502353—
CatalystHCID 178418397HCID 178418397—
ProductHCID 178466961HCID 178466961—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of [(S)-2-methyl-1-((S)-2-{4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-1H-imidazol-2-yl}-pyrrolidine-1-carbonyl)-propyl]-carbamic acid methyl ester (253 mg, 0.52 mmol) and the TFA salt of (R)-4-[5-(4-bromo-3-ethoxy-phenylcarbamoyl)-pyridin-2-yl]-3-methyl-piperazine-1-carboxylic acid tert-butyl ester (324 mg, 0.52 mmol; Preparation 21) was dissolved in 1,2-dimethoxyethane (5.32 mL, 51.2 mmol) and water (0.92 mL, 51.2 mmol) and the mixture was sparged under nitrogen. Sodium bicarbonate (161 mg, 1.92 mmol) was added, followed by tetrakis(triphenylphosphine)palladium(0) (89 mg, 0.077 mmol). The reaction mixture was further sparged with nitrogen, sealed under nitrogen and heated at 90° C. overnight. The reaction mixture was extracted with ethyl acetate and water. The organic layer was dried over sodium sulfate, filtered and concentrated to produce the title intermediate as a brown oil. (m/z): [M+H]+ calcd for C44H56N8O7 809.43 found 809.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260414B2
Source datasetuspto-grants-2016_02
ORD IDord-9a2fd11e8a5246bebac8c94da7c04f11
Source noteuspto-grants-2016_02