HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57156Generated: October 30, 2026
Benzenesulfonyl chloride → HCID 66906833, compound
https://huagongshe.com/reaction/57156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 66906974 | HCID 66906974 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 66906833 | HCID 66906833 | 36% |
Reaction Steps
To a solution of compound 145-H (0.46 g, 1.52 mmol) in pyridine (4.6 mL), cooled to 0° C., was added benzenesulfonyl chloride (0.206 mL, 1.60 mmol), and the reaction was heated to 50° C. for 72 h. Additional benzenesulfonyl chloride (0.412 mL, 3.20 mmol) was added and the reaction mixture was heated at 50° C. for an additional 16 h. The solvent was evaporated in vacuo, the residue dissolved in dichloromethane and washed with aqueous sodium bicarbonate. The aqueous layer was acidified with 1N HCl, extracted with dichloromethane, and the organic layer was evaporated in vacuo to afford a yellow solid (0.22 g, 36%) as a 1/3.5 mixture of the 3-bromo- and 3-chloro-substituted compounds, 145-Ia and 145-Ib, respectively. 1H-NMR (DMSO-d6): δ 7.1-7.2 (m, 1H), 7.4-7.6 (m, 3H), 7.8 (m, 2H), 8.1-8.2 (m, 1H), 8.25-8.35 (m, 1H); MS: m/z 465 and 509 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434711B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-83ab5dd2ade24808a966aa1072efd52c |
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| Source note | uspto-grants-2016_09 |
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