HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514876Generated: October 31, 2026
Cyanogen Bromide → 4-(2-Aminobenzo[d]thiazole-4-sulfonamido)benzoic acid
https://huagongshe.com/reaction/514876
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 4-(2-Amino-3-mercaptophenylsulfonamido)benzoic acid | HCID 90419018 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Aminobenzo[d]thiazole-4-sulfonamido)benzoic acid | HCID 90419092 | 100.9% |
Reaction Steps
To a solution of 4-(2-amino-3-mercaptophenylsulfonamido)benzoic acid (671 mg, 2.07 mmol) in THF (15 mL) was added cyanic bromide (439.1 mg, 4.14 mmol) at r.t. The reaction mixture was stirred at 80° C. for 8 h. The resulting mixture was then cooled, and partitioned between water and EtOAc. The organic phase was washed with brine, dried over anhy. Na2SO4 and concentrated in vacuo to afford the title compound (730 mg). LC-MS: m/z 348.7 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108921B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-415e914287084f788a0b7290dcdf5e21 |
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| Source note | uspto-grants-2015_08 |
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