HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563703Generated: October 30, 2026
Sodium methanethiolate → {2'-[(Cyclopropanecarbonyl-ethyl-amino)-methyl]-6-methoxy-4'-methylsulfanyl-biphenyl-3-yl}-acetic acid
https://huagongshe.com/reaction/563703
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | {2'-[(Cyclopropanecarbonyl-ethyl-amino)-methyl]-4'-fluoro-6-methoxy-biphenyl-3-yl}-acetic acid ethyl ester | HCID 58148989 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {2'-[(Cyclopropanecarbonyl-ethyl-amino)-methyl]-6-methoxy-4'-methylsulfanyl-biphenyl-3-yl}-acetic acid | HCID 44159059 | — |
Reaction Steps
To {2′-[(cyclopropanecarbonyl-ethyl-amino)-methyl]-4′-fluoro-6-methoxy-biphenyl-3-yl}-acetic acid ethyl ester 0.186 g, 0.45 mmol) in DMF (0.5 mL) was added sodium thiomethoxide (0.035 g, 0.50 mmol), and the reaction was stirred at 85° C. for 2 hours. Analytical LCMS indicated that starting material was still present, so additional sodium thiomethoxide (0.070 g, 1.0 mmol) was added, and the reaction was stirred at 85° C. for another 2 hours. Analytical LCMS showed that no starting material remained, and that the ethyl ester had been hydrolyzed, so an aqueous work-up was performed, and the residue was purified by preparative HPLC to give the title compound. M+H is 414.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067445B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b577b137740b4ec8b7ad83e9686d3a9b |
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| Source note | uspto-grants-2011_11 |
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