Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 86611703 | HCID 86611703 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86611704 | HCID 86611704 | — |
Reaction Steps
Water (8 mL) was added to a solution of 3-(bromomethyl)-6-chloroisothiazolo[5,4-b]pyridine (19.0 mmol) in dimethylsulfoxide (40 mL) and the reaction mixture was heated at 80° C. for 1.5 h. The reaction mixture was then quenched with water (50 mL) and the resulting solution was extracted with ethyl acetate (3×40 mL). The combined organic layers were dried (magnesium sulfate) and concentrated to provide the crude (6-chloroisothiazolo[5,4-b]pyridin-3-yl) methanol as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106066B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c8ace23114ed45648083a50a0e6f3842 |
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| Source note | uspto-grants-2012_01 |
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