HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923053Generated: October 30, 2026
4-Chloro-3-(pyridin-2-yl)aniline → HCID 58614831, compound
https://huagongshe.com/reaction/923053
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-3-(pyridin-2-yl)aniline | HCID 40151925 | — |
| Reactant | HCID 66967231 | HCID 66967231 | — |
| Product | HCID 58614831 | HCID 58614831 | — |
Reaction Steps
119 mg of (S)-styrene oxide was reacted with methyl 2-chloro-4-mercaptobenzoate via Procedure S to afford (S)-methyl 2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate. 230 mg of (S)-methyl-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoate was hydrolyzed via Procedure M to give (S)-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoic acid. 180 mg of (S)-2-chloro-4-(2-hydroxy-2-phenylethylthio)benzoic acid was reacted via Procedure R to give (S)-2-chloro-4-(2-hydroxy-2-phenylethylsulfonyl)benzoic acid. 60 mg of 4-chloro-3-(pyridine-2-yl)aniline was coupled to (S)-2-chloro-4-(2-hydroxy-2-phenylethylsulfonyl)benzoic acid via Procedure G. The product was purified on reverse phase HPLC to yield (S)-2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(2-hydroxy-2-phenylethylsulfonyl)benzamide. MS (Q1) 527.0 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278961B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-52b217360d304be1bce3e0057108ec92 |
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| Source note | uspto-grants-2016_03 |
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