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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350917Generated: November 3, 2026

Benzenesulfonyl chloride → HCID 69414949, compound

https://huagongshe.com/reaction/1350917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 69414844HCID 69414844—
SolventPyridineHCID 1049—
ProductHCID 69414949HCID 6941494999%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.10 mL (41 mmol) benzenesulphonic acid chloride were slowly added to a solution of 0.20 g (41 mmol) (R)-1-(3-amino-4-benzyloxyphenyl)-2-[1,1-dimethyl-3-(4-phenylimidazol-1-yl)-propylamino]-ethanol in 5 mL pyridine at 0° C. with vigorous stirring. After the addition was complete the reaction mixture was stirred for 4 h at 0° C. and then poured into 40 mL ice water/ethyl acetate (1:1). The phases were separated and the aqueous phase was extracted three times with 20 mL ethyl acetate. The combined organic phases were dried over magnesium sulphate and the solvent was removed using the rotary evaporator. 0.14 g (0.28 mmol, 99%) (R)—N-(2-benzyloxy-5-{2-[1,1-dimethyl-3-(4-phenylimidazol-1-yl)-propylamino]-1-hydroxyethyl}-phenyl)-benzenesulphonamide was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214698B2
Source datasetuspto-grants-2007_05
ORD IDord-b3649ec134ec48c2973bb8b3e5e0d562
Source noteuspto-grants-2007_05