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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122020Generated: October 30, 2026

Sodium Carbonate → HCID 9850181, compound

https://huagongshe.com/reaction/2122020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantHCID 69881524HCID 69881524—
ReactantHCID 69882484HCID 69882484—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 9850181HCID 9850181—

Reaction Steps

(2R,3S)-2-(4′-Methoxy-biphenyl-4-sulfonylamino)-3-(4-methyl-benzyloxy)-3-thiazol-2-yl-propionic acid methyl ester. The (2R,3S)-2-(4-bromo-benzenesulfonylamino)-3-(4-methyl-benzyloxy)-3-thiazol-2-yl-propionic acid methyl ester 1e (590 mg, 1.12 mmol) and 4-methoxyphenylboronic acid (260 mg, 1.68 mmol) are taken up in 10 mL of benzene, 1.5 mL of EtOH and 1.5 mL of water in the presence of Pd(PPh3)4 (40 mg, 0.03 mmol) and 237 mg of Na2CO3 and brought to reflux for 18 hours. The mixture is cooled to room temperature, poured into water, and extracted with methylene chloride. The organic layer is dried over Na2SO4, filtered and evaporated. The crude product is purified by silica gel chromatography using 6/4 hexane/EtOAc to give the desired product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696456B1
Source datasetuspto-grants-2004_02
ORD IDord-fb77c0f4453e49ea92e1a8865471aef6
Source noteuspto-grants-2004_02