HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49142Generated: October 29, 2026
Sodium Methoxide → 5-[[2-[N-(6-Bromopyridin-2-yl)amino]thiazol-5-yl]thio]-2-methylbenzoic acid
https://huagongshe.com/reaction/49142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-Mercapto-2-methyl-benzoic acid | HCID 15404466 | — |
| Reactant | 6-Bromo-n-(5-bromo-2-thiazolyl)pyridin-2-amine | HCID 22170424 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[[2-[N-(6-Bromopyridin-2-yl)amino]thiazol-5-yl]thio]-2-methylbenzoic acid | HCID 22170384 | 81.3% |
Reaction Steps
A suspension of 2-[(6-bromo-2-pyridinyl)amino]-5-bromothiazole (100 mg, 0.3 mmol), 3-carboxy-4-methylthiophenol (170 mg, 0.98 mmol) and sodium methoxide (210 μL, 25% w/w solution in methanol, 0.9 mmol) in methanol (4.9 mL) and THF (2 mL) was heated to 54° C. for 5.5 h. Supplemental sodium methoxide solution (1.42 mL) was added in portions over a period of 5 h. The mixture was heated to 54° C. for 16 h and concentrated. The residue was diluted with 1 N aqueous HCl solution at 0° C. and stirred for several minutes. The precipitated solid was filtered, washed several times with water and ether, and dried in vacuo over P2O5. Trituration with ether afforded the titled compound (103 mg, 81%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706717B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-ef954bfc615b4c038770449f1a96e266 |
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| Source note | uspto-grants-2004_03 |
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