HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177484Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 178525791, compound
https://huagongshe.com/reaction/1177484
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | HCID 44601274 | HCID 44601274 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178525791 | HCID 178525791 | — |
Reaction Steps
3-((3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)phenyl)methyl)-cyclobutane-1,1-dicarboxylic acid (0.360 g, 0.716 mmol) was treated with 4 mL DMSO, fitted with a water cooled reflux condenser, and heated to 160° C. After 4 h, the reaction mixture was cooled to rt. The reaction mixture was partitioned between water and EtOAc. The organic layer was washed with water once, satd NaCl once and the organics were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give a light yellow solid, as an approximately 2:1 mixture of isomers. Separation by SFC (Gradient with Chiralpak IC (21×250 mm, 5 micron), pure methanol with CO2 70 mL/min) gave (trans)-3-(3-fluoro-4-(5-(1-phenylcyclopropyl)-thiazolo[5,4-b]pyridine-2-yl)benzyl)cyclobutanecarboxylic acid as a white solid. MS (ESI) m/z: calculated: 458.2; Observed: 459.1 (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-cb0a9be6c73f4c3297388e7ffe68c273 |
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| Source note | uspto-grants-2010_11 |
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