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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427859Generated: November 3, 2026

Triethylamine → HCID 74834218, compound

https://huagongshe.com/reaction/2427859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 74823169HCID 74823169—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 74834218HCID 7483421825.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude benzoic acid 2-(3,5-dichloro-pyridin-4-yl)-1-(4-methoxy-8-amino-dibenzofuran-1-yl)-vinyl ester (1.17 g, obtained as described in Example 8 starting from 1.68 g of benzoic acid 2-(3,5-dichloro-pyridin-4-yl)-1-(4-methoxy-8-nitro-dibenzofuran-1-yl)-vinyl ester) is dissolved in dry DCM (5 mL) under nitrogen atmosphere. The solution is cooled to 0° C. and triethylamine (0.390 mL, 2.80 mmoles) and methanesulphonyl chloride (0.220 mL, 2.83 mmoles) are added sequentially dropwise. The resulting solution is stirred at room temperature for 1 hour. The mixture is diluted with water (2.5 mL) and saturated NaHCO3 solution (10 mL) and extracted with DCM; the combined organic layers are dried over Na2SO4 and evaporated to dryness. The crude is purified by preparative HPLC to yield 330 mg of pure product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968724B2
Source datasetuspto-grants-2011_06
ORD IDord-49887ccc4b4641aca2fb3ed0514cdf06
Source noteuspto-grants-2011_06