Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 18536895 | HCID 18536895 | — |
| Reactant | HCID 18537238 | HCID 18537238 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69939571 | HCID 69939571 | 82% |
Reaction Steps
5-Methylthio-4-(4-phenyl(1,3-oxazol-2-yl))thiophene-2-carboxamidine hydrochloride: Methyl 5-methylthio-4-(4-phenyl(1,3-oxazol-2-yl))thiophene-2-carboxylate (80.3 mg, 0.242 mmol, as prepared in the previous step) was treated according to the procedure in Example 10, step (b) using 155 mg (2.90 mmol) of ammonium chloride in 1.45 mL of toluene and 1.45 mL (2.90 mmol) of 2 M trimethylaluminum in toluene. The resulting light yellow solid was chromatographed on a 5 g silica SPE column (Waters Sep-Pak) with 10% MeOH—CH2Cl2 to give a light yellow resin. Crystallization from MeOH—Et2O (ca. 1:3) afforded the title compound as a yellow solid (62.2 mg, 82%). 1H-NMR (300 MHz, DMSO-d6) δ 9.39 (broad s, 2H), 8.97 (broad s, 2H), 8.78 (s, 1H), 8.60 (s, 1H), 7.89 (d, 2H, J=7 Hz), 7.49 (t, 2H, J=7 Hz), 7.38 (t, 1H, J=7 Hz), and 2.80 (s, 3H). Mass spectrum (ESI) calcd. for C15H13N3OS2: 316.1(M+H). Found: 316.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515002B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-21b17503551d4b43a7b6acb08761d29b |
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| Source note | uspto-grants-2003_02 |
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