Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 18537031 | HCID 18537031 | — |
| Reactant | HCID 18537479 | HCID 18537479 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18537269 | HCID 18537269 | — |
Reaction Steps
5-Methylthio-4-(phenylsulfonyl)thiophene-2-carboxamidine trifluoroacetate: The same procedure as in Example 257, step (b) was followed using 13.8 mg (0.044 mmol) of methyl 5-methylthio-4-(phenylsulfonyl)thiophene-2-carboxylate (as prepared in the step before), 20 mg of ammonium chloride (0.376 mmol), 0.176 ml of trimethylaluminum (2.0 M in toluene, 0.353 mmol) and 3 ml of anhydrous toluene and chromatographed as before by preparative reverse phase HPLC performed with a Rainin SD-1 Dynamax system and a 2-in. C18 reverse phase Dynamax 60A column using a gradient of 30% MeOH/0.1% TFA in water to 100% MeOH and a flow rate of 50 mL/min to yield 2.3 mg of 5-methylthio-4-(phenylsulfonyl)thiophene-2-carboxamidine. 1H-NMR (CD3OD, 400 MHz) δ 8.42 (s, 1H), 8.04 (m, 2H), 7.70 (m, 2H), 7.62 (m, 1H) and 2.70 (s, 3H). Mass spectrum (ESI, m/z): Calcd. C12H12N2O2S3, 313.0 (M+H), found 313.2.
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-04a09f3c831a4b1ea62b7ea04cc3e7c6 |
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| Source note | uspto-grants-2003_02 |
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