HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061549Generated: November 1, 2026
4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide → 4-Amino-3-nitro-N-(3-pyridinylmethyl)benzenesulfonamide
https://huagongshe.com/reaction/1061549
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide | HCID 2858305 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Product | 4-Amino-3-nitro-N-(3-pyridinylmethyl)benzenesulfonamide | HCID 22285168 | — |
Reaction Steps
Into a saturated ammonia-methanol solution (60 ml) was added 4-chloro-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide (2.77 g), followed by about 2 days of heating at 100° C. in a sealed tube. After the reaction, the solvent was evaporated under reduced pressure and the formed yellow crystals were collected by filtration and dried to obtain 4-amino-3-nitro-N-(pyridin-3-ylmethyl)benzenesulfonamide (2.51 g). Hereinafter, the compound of Reference Examples 26 was obtained similarly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960591B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-9f9472e3325a4e56940e70a7170ae712 |
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| Source note | uspto-grants-2005_11 |
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