HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044756Generated: October 31, 2026
Nitrogen → (5-(2-Methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl)methyl methanesulfonate
https://huagongshe.com/reaction/1044756
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 (500 mg, 2.48 mmol) in dry CH2Cl2 (15 mL) was treated at 0° C. with Et3N (0.45 mL, 3.21 mmol) followed by DMAP (31 mg, 0.25 mmol) and Ms-Cl (0.25 mL, 3.14 mmol). After stirring at 0° C. for 1 h, the reaction was quenched with water (10 mL). The org. layer was dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give crude (5-(2-methyl-[1,3]dioxolan-2-yl)-thiazol-2-yl)methyl methanesulfonate as a brown oil. This material was dissolved in dry DMF (10 mL) and treated with NaN3 (175 mg, 2.66 mmol) at 80° C. until completion of the reaction. The reaction mixture was then cooled down to rt and partitioned between EA and water. The layers were separated and the org. layer dried over MgSO4, filtered and concentrated under reduced pressure to give crude 2-(azidomethyl)-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazole as a yellow oil. LC-MS-conditions 02: tR=0.86 min; [M+H]+=227.47.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563714B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d8108525e5c646bdb46542ba88a80a60 |
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| Source note | uspto-grants-2013_10 |
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