HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898292Generated: November 3, 2026
HCID 58268353, compound → HCID 44178160, compound
https://huagongshe.com/reaction/1898292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58268353 | HCID 58268353 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 44178160 | HCID 44178160 | — |
Reaction Steps
A mixture of N-{2-[1-(tert-Butyl-dimethyl-silanyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonyl]-5-chloro-6-methyl-pyridin-3-yl}-4-chloro-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide (from above step) in 2 ml of 4M HCl and 2 ml of dioxane was stirred at 90° C. for 2 hours. The mixture was concentrated and the residue was diluted with ethyl acetate, this organic layer was washed with saturated sodium bicarbonate and followed by brine and then dried over sodium sulfate. After filtration and concentration the residue was purified by preparative TLC to afford the title compound. 1H NMR: (CD3OD, ppm): 8.15 (d, 1H), 7.98 (s, 1H), 7.84 (m, 1H), 7.53 (m, 1H), 7.40 (d, 1H), 7.26 (d, 1H), 7.07 (d, 1H), 6.23 (d, 1H), 2.47 (s, 3H); MS (ES) (M++H) expect 529. found 528.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519135B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-4118b1f6a8bd4f0a945fc5f4731d2772 |
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| Source note | uspto-grants-2013_08 |
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