HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077503Generated: November 2, 2026
2-Fluorobenzenesulphonyl chloride → HCID 57584938, compound
https://huagongshe.com/reaction/2077503
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluorobenzenesulphonyl chloride | HCID 137761 | — |
| Reactant | HCID 57585060 | HCID 57585060 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57584938 | HCID 57584938 | — |
Reaction Steps
N-(6-(6-Aminopyridin-2-yl)benzo[d]thiazol-2-yl)acetamide (0.220 g, 0.775 mmol) was dissolved in DMSO (3 mL). TEA (0.3 mL, 2 mmol), DMAP (0.020 g, 0.16 mmol), and 2-fluorobenzene-1-sulfonyl chloride (0.4 mL, 3 mmol) were added to the mixture while stirring. The mixture was allowed to stir under inert atmosphere overnight and then it was diluted with DMSO and purified by reverse phase HPLC to give N-(6-(6-(2-fluorophenylsulfonamido)pyridin-2-yl)benzo[d]thiazol-2-yl)acetamide as a yellow solid. MS (ESI pos. ion) m/z: 443 (MH+). Calculated exact mass for C21H15FN4O3S2: 442. 1H NMR (400 MHz, DMSO-d6): 7.99 (s, 1H), 7.94 (t, J=7.3 Hz, 1H), 7.68 (d, J=8.5 Hz, 1H), 7.32-7.47 (m, 3H), 7.28 (t, J=7.5 Hz, 1H), 7.21 (t, J=7.8 Hz, 1H), 7.10 (d, J=7.5 Hz, 1H), 6.41 (d, J=8.5 Hz, 1H), 2.10 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928140B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-43473347b92b4acfbdf72c3adc755931 |
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| Source note | uspto-grants-2011_04 |
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