HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984710Generated: November 2, 2026
Water → 2-Acetylamino-4-methanesulfonyloxymethylpyridine
https://huagongshe.com/reaction/1984710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-(4-(hydroxymethyl)pyridin-2-yl)acetamide | HCID 23151114 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Acetylamino-4-methanesulfonyloxymethylpyridine | HCID 23151034 | 87% |
Reaction Steps
A solution of triethylamine (1.7 mL, 12 mmol) and methanesulfonyl chloride (0.70 mL, 9.0 mmol) in anhydrous tetrahydrofuran (3.0 mL) was added to a solution of (2-acetylaminopyridin-4-yl)methanol (Reference compound No. 12-1, 1.0 g, 6.0 mmol) in anhydrous tetrahydrofuran (9.0 mL) under ice-cooling, and the mixture was stirred for 20 minutes. Water (30 mL) was added to the reaction mixture, the whole was extracted with ethyl acetate (40 mL) three times, and then the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting solid was filtered off with hexane. The solid was dried under reduced pressure at 40° C. to give 1.3 g of the title reference compound as a pale yellow solid. (Yield 87%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07544703B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-aadaa508f2b74bc1a956ff5a6c05eb4a |
|---|
| Source note | uspto-grants-2009_06 |
|---|