HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364762Generated: November 1, 2026
4-Chloro-3-(pyridin-2-yl)aniline → HCID 58614696, compound
https://huagongshe.com/reaction/1364762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-(pyridin-2-yl)aniline | HCID 40151925 | — |
| Reactant | HCID 66877317 | HCID 66877317 | — |
| Product | HCID 58614696 | HCID 58614696 | — |
Reaction Steps
175 μL of 1-iodo-2-methylpropane and 740 mg of Cesium Carbonate were added to 200 mg of methyl 2-chloro-4-(methylsulfonamido)benzoate in 2 mL of DMF and stirred in the microwave at 140° C. for 30 minutes. The reaction mixture was extracted in Ethyl Acetate twice with water, dried over Magnesium Sulfate, filtered, concentrated and purified on ISCO Combi-Flash to give methyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoate. 120 mg of methyl 2-chloro-4-(N-isobutylmethylsulfonamido)benzoate was hydrolyzed via Procedure M to yield 110 mg of crude 2-chloro-4-(N-isobutylmethylsulfonamido)benzoic acid. 75 mg of 4-chloro-3-(pyridin-2-yl)aniline was coupled to 2-chloro-4-(N-isobutylmethylsulfonamido)benzoic acid via Procedure G. The crude product was purified by reverse phase HPLC to yield 2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(N-isobutylmethylsulfonamido)benzamide. MS (Q1) 492 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888364B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-97154b99ddb44e3b80dd557bb3951a1f |
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| Source note | uspto-grants-2011_02 |
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