Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 10383831 | HCID 10383831 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86594315 | HCID 86594315 | — |
Reaction Steps
A stirred suspension of (E)-2-(4-nitrophenyl)-3-(tetrahydropyran-4-yl)-N-thiazol-2-ylacrylamide (EXAMPLE 81, 1.54 g, 4.0 mmol) in EtOH (54 mL) and THF (31 mL) was treated with H2O (13 mL), saturated aqueous NH4Cl (13 mL), and Fe powder (1.49 g, 26.7 mmol). After 4.5 h at 20° C., the reaction mixture was filtered through Celite, washing with CH2Cl2. The combined filtrates were concentrated and the residue was dissolved in CH2Cl2. The CH2Cl2 solution was washed with H2O and dried (MgSO4). Filtration, solvent evaporation, and column chromatography (EtOAc-MeOH, 19:1) gave (E)-2-(4-aminophenyl)-3-(tetrahydropyran-4-yl)-N-thiazol-2-ylacrylamide: m/z (ES+)=330.1 [M+H]+. A stirred solution of this compound (104 mg, 291 μmol) in anhydrous CH2Cl2 (4 mL) was treated with MeSO2Cl (90 μL, 1165 μmol) and pyridine (94 μL, 1165 μmol). After 16 h, the mixture was diluted with CH2Cl2 (25 mL), before being extracted twice with 2M NaOH. The combined aqueous extracts were washed with Et2O, before being acidified with 12M HCl to pH1 and extracted twice with CH2Cl2. The combined organic extracts were washed with brine and dried (MgSO4). Filtration and solvent evaporation afforded the title compound: RTB=1.26 min; m/z (ES+)=408.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214681B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-912de40d7d7948abb8fbe2008d267826 |
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| Source note | uspto-grants-2007_05 |
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