HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177437Generated: November 1, 2026
Ozone → (2-(4-(1,3-Dioxan-2-yl)-2-fluorophenyl)thiazolo[5,4-b]pyridine-5-yl)(phenyl)methanone
https://huagongshe.com/reaction/1177437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ozone | HCID 24823 | — |
| Reactant | 2-(4-(1,3-Dioxan-2-yl)-2-fluorophenyl)-5-(1-phenylvinyl)thiazolo[5,4-b]pyridine | HCID 67111819 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | (2-(4-(1,3-Dioxan-2-yl)-2-fluorophenyl)thiazolo[5,4-b]pyridine-5-yl)(phenyl)methanone | HCID 67111595 | — |
Reaction Steps
A solution of 2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)-5-(1-phenylvinyl)thiazolo[5,4-b]pyridine (2.66 g, 6.4 mmol) in 3:1 CH2Cl2/MeOH (128 mL) at −78° C. was treated with ozone for 15 min. The solution was then sparged with O2, dimethyl sulfide (18 mL) was added, and the bath was allowed to expire. The resulting solution was stirred at 25° C. for 3 d and then concentrated in vacuo. This residue was taken up in CH2Cl2 (400 mL) and sequentially washed with water and brine, then concentrated in vacuo to provide (2-(4-(1,3-dioxan-2-yl)-2-fluorophenyl)thiazolo[5,4-b]pyridine-5-yl)(phenyl)methanone as a yellow solid. MS (ESI) m/z: Calculated: 420.1; Observed: 421.1 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842685B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-35a939e66b454657a497732406409882 |
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| Source note | uspto-grants-2010_11 |
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