HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943232Generated: October 27, 2026
Water → [1,2,5]Thiadiazolo[3,4-b]pyridine-6-carbaldehyde
https://huagongshe.com/reaction/1943232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | 6-[(E)-2-Phenylethenyl][1,2,5]thiadiazolo[3,4-b]pyridine | HCID 68596316 | — |
| Catalyst | Water | HCID 962 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [1,2,5]Thiadiazolo[3,4-b]pyridine-6-carbaldehyde | HCID 82414701 | — |
Reaction Steps
To 6-[(E)-2-phenylethenyl][1,2,5]thiadiazolo[3,4-b]pyridine (0.88 g, 3.68 mmol) was added acetone (30 ml), N-methyl-morpholine-N-oxide, 50 wt. % in water (1.525 ml, 7.35 mmol) and then osmium tetroxide in water (0.225 ml, 0.037 mmol). The reaction was then stirred for 20 hours. To the pale brown solution was added sodium periodate (3.15 g, 14.71 mmol) and stirring continued for 45 mins. The solvent was reduced by rotary evaporation and the remainder partitioned between chloroform and water. The aqueous was further extracted with chloroform and the combined organic extracts passed through a hydrophobic frit and concentrated to give brown/black solid (0.6 g). A portion of this material (0.575 g) was purified by chromatography on silica eluting with 20% EtOAc in cyclohexane to a pale yellow solid (160 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389524B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-c6af9bcf5f2141ba9d52ca1a3bb07de5 |
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| Source note | uspto-grants-2013_03 |
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