HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049024Generated: October 31, 2026
Diisopropylethylamine → 4-{5-[(4-Fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1049024
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | 6-Chloro-pyridine-3-sulfonic acid (4-fluoro-phenyl)-isobutyl-amide | HCID 86721875 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-{5-[(4-Fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl ester | HCID 86721876 | 31% |
Reaction Steps
To a solution of 6-chloro-pyridine-3-sulfonic acid (4-fluoro-phenyl)-isobutyl-amide (150 mg, 439 μmol) and 4-amino-1-boc piperidine (114 mg, 570 μmol) in acetonitrile (3 mL) was added DIPEA (115 μl, 658 μmol) and the reaction was heated at 160° C. in a microwave reactor for 2.5 hours. EtOAc and saturated aqueous NaHCO3 were added, extracted, washed with brine, dried with Na2SO4 then concentrated and purified by silica gel column chromatography (0-50% EtOAc in cyclohexane) to give 4-{5-[(4-fluoro-phenyl)-isobutyl-sulfamoyl]-pyridin-2-ylamino}-piperidine-1-carboxylic acid tert-butyl ester (69 mg, 31%). LCMS (m/z, Method A) ES− 506 [M−1]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382222B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-9e998b1fde03419e8ab94903b300f7a4 |
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| Source note | uspto-grants-2016_07 |
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