HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259525Generated: November 1, 2026
Triethylamine → 5-(((Methanesulfonyl)oxy)methyl)-2-methylthiazolo[5,4-b]pyridine
https://huagongshe.com/reaction/2259525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-methylThiazolo[5,4-b]pyridine-5-methanol | HCID 19002884 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(((Methanesulfonyl)oxy)methyl)-2-methylthiazolo[5,4-b]pyridine | HCID 22068764 | — |
Reaction Steps
To a solution of the alcohol of Step 6 (303 mg, 1.68 mmol) in 17 mL of CH2Cl2 at -40° C., triethylamine (350 μl, 2.5 mmol) and methane-sulfonyl chloride (170 μl, 2.2 mmol) were added and the solution was stirred at -40° C. for 30 min and at 0° C. for 2 hr. Saturated aq. NaHCO3 was added and the product was extracted in CH2C12, dried over Na2SO4, concentrated, and the remaining water was stripped with toluene twice.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05472964 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-61836e9bf8f24e73a97f3cc854334b1f |
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| Source note | uspto-grants-1995_12 |
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