HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966212Generated: October 31, 2026
Disodium disulfite → HCID 25261021, compound
https://huagongshe.com/reaction/1966212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Disodium disulfite | HCID 24346 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 25261019 | HCID 25261019 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25261021 | HCID 25261021 | 44% |
Reaction Steps
(5-Phenylsulfanyl-pyridine-2-yl)-thiazole-2-yl-amine (0.13 mmol) is dissolved in dichloromethane, cooled to 0° C. and m-chloro-perbenzoic acid (1 eq.) is added. The reaction is stirred 30 min at 0° C. and 2.5 hours at RT. Sodium disulfite (50 ml) is added and extracted with dichloromethane. The combined organic layers are washed with saturated NaHCO3, dried over MgSO4 and the solvent is removed in vacuo. “A13” is obtained after reversed phase column chromatography (water/acetonitrile) as a yellow powder in a yield of 44% HPLC (method C): 1.41 min; LC-MS (method A): 1.223 min, 301.95 (M+H+); 1H-NMR (DMSO-d6, 500 MHz): δ [ppm] 11.657 (s, 1H), 8.634-8.628 (m, 1H), 7.853 (dd, 1H, J=2.4 Hz, J=8.9 Hz), 7.722-7.703 (m, 2H), 7.583-7.507 (m, 3H), 7.425 (d, 1H, J=3.6 Hz), 7.152 (d, 1H, J=8.9 Hz), 7.100 (d, 1H, J=3.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420642B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-43d2010b2ece4fa3ae1bbd5a615ee0b7 |
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| Source note | uspto-grants-2013_04 |
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