Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 91335761 | HCID 91335761 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69319218 | HCID 69319218 | 53.3% |
Reaction Steps
To a solution of methyl[2-(5-acetyl-2-methoxy-benzylsulfanyl)-6-fluoro-benzoimidazol-1-yl]-acetate (Precursor 6-F-H-11b, 11.3 mg, 0.029 mmol) in dry THF (0.3 ml) is added some 1 N aqueous lithium hydroxide solution (0.140 ml, 5 eq.). The resulting biphasic solution is allowed to stir 1 h at rt. The solvents are removed in vacuo, water is added as well as 1N HCl in water so as to set the pH of the aqueous solution to pH=1. The resulting acidic aqueous phase is extracted three times with AcOEt. The organic phase is dried over Na2SO4 and the solvent removed in vacuo and the product was dried under high vacuum. This yields the title compound (6 mg) in 55% as a greyish solid: tR=0.95 min (LC-3), ESI-MS (pos.): m/z 388.89 [M+H]+, ESI-MS (neg.): m/z 387.10 [M−H]+; 1H-NMR (DMSO-d6): δ (ppm) 2.40 (s, 3H, COCH3), 3.87 (s, 3H, OCH3), 4.49 (s, 2H, SCH2), 4.82 (s, 2H, CH2CO2), 7.01 (t, 1Harom), 7.09 (d, 1Harom), 7.42 (d, 1Harom), 7.53 (dd, 1Harom), 7.86 (d, 1Harom), 7.98 (s, 1Harom).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273740B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-ae37fd1065684979a6b8b1b942ac9bd0 |
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| Source note | uspto-grants-2012_09 |
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