HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641841Generated: October 30, 2026
Methanesulfonyl chloride → HCID 59259093, compound
https://huagongshe.com/reaction/641841
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 45091313 | HCID 45091313 | — |
| Reactant | (2-Amino-5-(prop-2-yn-1-yloxy)phenyl)(4-isopropylphenyl)methanone | HCID 45139628 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59259093 | HCID 59259093 | — |
Reaction Steps
To a solution of 400 mg (2.18 mmol) [2-(2-methoxy-ethoxy)-pyridin-3-yl]-methanol in 4 ml dioxane at r.t. is added 1.12 ml (6.55 mmol) Hünig's base followed by 170 μl (2.18 mmol) mesyl chloride and the mixture is stirred for 5 min. 641 mg (2.18 mmol) (2-amino-5-propargyloxy-phenyl)-(4-isopropyl-phenyl)-methanone is added to this mixture with the addition of 1 ml of dioxane. The reaction mixture is then heated to 100° C. and stirred overnight. The mixture is partitioned between ether/water and the organic layer is washed with brine, dried with Na2SO4, filtered and evaporated. Flash-chromatography (ethyl acetate/ether 1:1) yields a yellow oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696216B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-26595e5e427149e4909ef964a34f7fa9 |
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| Source note | uspto-grants-2010_04 |
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