HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466913Generated: October 29, 2026
Methanesulfonamide → HCID 67831691, compound
https://huagongshe.com/reaction/466913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 14853399 | HCID 14853399 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67831691 | HCID 67831691 | 58.6% |
Reaction Steps
To a solution of 1,1-carbonyldiimidazole (1.70 g, 0.0105 mol) in dry tetrahydrofuran (130 ml), 2-(4,6-dimethoxypyrimidin-2-yl)oxypropionic acid (2.28 g, 0.01 mol), prepared as described in Example 1(b) above, in tetrahydrofuran (30 ml) was added dropwise at room temperature (~20° C.). The solution was refluxed for 1/2 hour and allowed to cool. Methanesulphonamide (0.95 g, 0.01 mol) was added in one solid portion and the mixture stirred for 15 minutes before 1,8-diazabicyclo[5.4.0]undec-7-ene (1.52 g, 0.01 mol) in tetrahydrofuran (30 ml) was added dropwise at room temperature (~20° C.). After a short duration the tetrahydrofuran was removed and the residue acidified with IM hydrochloric acid solution. The product was extracted with chloroform, backwashed with water and dried. The solvent was removed and the product purified on silica gel eluting with 3% by volume methanol/chloroform to yield the title compound as a solid (1.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158599 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-e44d0f8767de49e9a1565e972c554ae3 |
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| Source note | uspto-grants-1992_10 |
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