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| | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate Basic information | | Uses |
| Product Name: | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate | | Synonyms: | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate;tert-butyl (S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate;1-Pyrrolidinecarboxylic acid, 2-(5-bromo-1H-imidazol-2-yl)-, 1,1-dimethylethyl ester, (2S)-;tert-butyl (2S)-2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate;tert-butyl (2S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate;EOS-61040;(S)-tert-butyl 2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate;tert-Butyl (S)-2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate | | CAS: | 1007882-59-8 | | MF: | C12H18BrN3O2 | | MW: | 316.19 | | EINECS: | 813-157-2 | | Product Categories: | | | Mol File: | 1007882-59-8.mol |  |
| | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate Chemical Properties |
| Boiling point | 469.3±35.0 °C(Predicted) | | density | 1.444±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 11.13±0.10(Predicted) | | Appearance | White to off-white Solid | | InChI | InChI=1S/C12H18BrN3O2/c1-12(2,3)18-11(17)16-6-4-5-8(16)10-14-7-9(13)15-10/h7-8H,4-6H2,1-3H3,(H,14,15)/t8-/m0/s1 | | InChIKey | GAZHEEFWONCMGH-QMMMGPOBSA-N | | SMILES | N1(C(OC(C)(C)C)=O)CCC[C@H]1C1NC(Br)=CN=1 |
| | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate Usage And Synthesis |
| Uses | It can be used as a chemical and pharmaceutical intermediate in the laboratory research and development process. | | Synthesis | To a preparation of (S)-tert-butyl 2-(4,5-dibromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (12.5 g, 31.5 mmol) in a mixture of dioxane (400 ml) and H2O (400 ml) was added a solution of Na2SO3 (43.7 g, 347 mmol) in H2O (400 ml) and heated to reflux for 21 hours. The mixture was concentrated to half volume and extracted with CH2Cl2 (3 x 200 ml). The organics were then washed with brine, dried (MgSO4), filtered and concentrated. Purification by grinding (CH2Cl2, tBuOMe, and hexane) afforded 5.2 g (52%) of tert-butyl (S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate. MS (ESI) m/z 317(M+H)+. |
| | (S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate Preparation Products And Raw materials |
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