HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599476Generated: October 31, 2026
Potassium Carbonate → HCID 67032056, compound
https://huagongshe.com/reaction/599476
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-1-propanol | HCID 12308 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-[4-(3,5-di-tert-butyl-4-hydroxy-phenylsulfanyl)-piperidine-1-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester | HCID 86635430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67032056 | HCID 67032056 | 42.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897776B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-faec37cb3c7745f390aeae08f82b2ee8 |
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| Source note | uspto-grants-2011_03 |
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