HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366834Generated: October 31, 2026
2,4-Dichloro-5-methylbenzene-1-sulphonyl chloride → HCID 57718252, compound
https://huagongshe.com/reaction/1366834
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichloro-5-methylbenzene-1-sulphonyl chloride | HCID 119914 | — |
| Reactant | 2-Amino-5-bromo-4-methylpyridine | HCID 817695 | — |
| Reactant | 4-(N-piperidinylsulfonyl)thiophenol | HCID 57718290 | — |
| Product | HCID 57718252 | HCID 57718252 | — |
Reaction Steps
2,4-Dichloro-5-methyl-N-{4-methyl-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-pyridin-2-yl}-benzenesulfonamide was prepared from 2-amino-5-bromo-4-methylpyridine and 4-(N-piperidinylsulfonyl)thiophenol according to General Method 11 step 1 followed by reaction with 2,4-dichloro-5-methylphenylsulfonyl chloride according to General Method 11 step 2. 1H NMR (CDCl3): 13.20 (1 H, br s, NH), 8.40 (1 H, s, A-ring CH ortho to 2×Cl), 8.03 (1 H, s, A-ring CH ortho to SO2NH), 7.53 & 7.04 (2×2 H, 2×d, 2×J 10 Hz, Ar CH's of C-ring), 7.41 & 7.15 (2×1 H, 2×s, pyridyl CH's), 2.91-2.83 (4H, m, CH2NCH2), 2.38 & 2.23 (2×3H, 2×s, 2×CH3), 1.61-1.48 (4 H, m, CH2CH2CH2CH2CH2), 1.39-1.28 (2 H, m, CH2CH2CH2CH2CH2). Hplc (Luna 2, Gradient 5): rt=6.73 minutes. LC/MS rt=7.43 minutes, 586/588 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893077B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-0614ba08202646e4826d733930235fcd |
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| Source note | uspto-grants-2011_02 |
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