HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42840Generated: October 28, 2026
Nitrogen → (5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl)methyl methanesulfonate
https://huagongshe.com/reaction/42840
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | [5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl]-methanol | HCID 66819954 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl)methyl methanesulfonate | HCID 86649489 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of [5-(2-methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl]-methanol (560 mg, 2.78 mmol) in dry CH2Cl2 (5.0 mL) was treated at 0° C. with Et3N (0.50 mL, 3.60 mmol) followed by DMAP (34 mg, 0.28 mmol) and Ms-Cl (0.28 mL, 3.51 mmol). After stirring at 0° C. for 1 h, the reaction mixture was quenched with water (10 mL), extracted with CH2Cl2 (10 mL) and the combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (5:1 to 2:1 hept-EA) gave the title compound as a brown oil. LC-MS-conditions 01: tR=0.77 min; [M+H]+=279.88.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536209B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-491133adc4a34fb5be4e02051ba2e319 |
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| Source note | uspto-grants-2013_09 |
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