HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054476Generated: October 30, 2026
HCID 62916801, compound → HCID 118590304, compound
https://huagongshe.com/reaction/1054476
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 62916801 | HCID 62916801 | — |
| Reactant | HCID 118590531 | HCID 118590531 | — |
| Product | HCID 118590304 | HCID 118590304 | — |
Reaction Steps
The title compound was prepared by the method similar to that of Example 31 employing 4-(3-hydroxypyrrolidin-1-yl)benzene sulfonamide (Int-51) and 6-(2-(2,5-difluorophenyl)piperidin-1-yl)imidazo[1,2-a]pyridine-3-carboxylic acid (Int 23) to afford an enantiomeric mixture which was purified by column chromatography using CHIRALPAK AD-H column and n-HEXANE:ETHANOL, 80:20 isocratic solution as eluent to afford 6-(2-(2,5-difluorophenyl)piperidin-1-yl)-N-((4-((S)-3-hydroxypyrrolidin-1-yl)phenyl)sulfonyl)imidazo[1,2-a]pyridine-3-carboxamide (0.012 g) (Isomer-II) MS (ESI): m/z 582.2 (M+H); 1H NMR (400 MHz, DMSO-d6) δ 12.00 (1H, S), 8.83 (1H, s), 8.4 (1H, s), 7.76-7.74 (2H, m), 7.58-7.56 (1H, m), 7.46-7.43 (1H, m), 7.07-6.99 (2H, m), 6.91-6.90 (1H, m), 6.65-6.62 (1H, m), 5.04-5.03 (1H, d), 4.42 (2H, bs), 3.50-3.38 (4H, m), 3.28-3.20 (1H, m), 2.90-2.85 (1H, m), 2.06-2.03 (1H, m), 1.91-1.88 (3H, m), 1.76-1.67 (1H, m), 1.64-1.53 (1H, m) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394305B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-fa4651ceb8f646ca8f4fbf30e1917005 |
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| Source note | uspto-grants-2016_07 |
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