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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599476Generated: October 31, 2026

Potassium Carbonate → HCID 67032056, compound

https://huagongshe.com/reaction/599476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-1-propanolHCID 12308—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-[4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidine-1-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylic acid methyl esterHCID 86635430—
SolventDimethylformamideHCID 6228—
ProductHCID 67032056HCID 6703205642.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

To 5-[4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidine-1-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester (Ex. 4a, 436 mg, 0.83 mmol) in 3 mL of DMF was added 3-bromo-propan-1-ol (127 mg, 0.91 mmol) and K2CO3 (343 mg, 2.5 mmol). The mixture was heated to 75° C. for 16 h. Upon cooling to room temperature it was poured into saturated NH4Cl (30 mL). The mixture was extracted with Ethyl acetate (3×30 mL) and the organic extracts were dried over Na2SO4 and concentrated under reduced pressure. Chromatography (3-40% Ethyl acetate/hexanes) gave 5-{4-[3,5-di-tert-butyl-4-(3-hydroxy-propoxy)-phenylsulfanyl]-piperidine-1-sulfonyl}-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester as a pale-yellow thick oil (203 mg). ESI/CI-MS m/z 581 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897776B2
Source datasetuspto-grants-2011_03
ORD IDord-faec37cb3c7745f390aeae08f82b2ee8
Source noteuspto-grants-2011_03