Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 2-(Bromomethyl)tetrahydro-2H-pyran | HCID 141917 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | 3-((tetrahydro-2H-pyran-2-yl)methyl)thiazol-2(3H)-imine | HCID 68623066 | — |
Reaction Steps
A mixture of 2-aminothiazole (1.0 g, 10 mmol) and 2-(bromomethyl)tetrahydro-2H-pyran (1.3 mL, 10 mmol) was warmed to 85° C. and was allowed to stir for 24 hours. The mixture was cooled to ambient temperature and the crude material was purified via column chromatography (SiO2, 10% methanol in ethyl acetate then 9:1:0.1 CH2Cl2:methanol:NH4OH) to afford the title compound. MS (DCI/NH3) m/z 199 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08546583B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-447154c4aeb242dcb87d360f91bbc890 |
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| Source note | uspto-grants-2013_10 |
|---|
