Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phenylsilane | HCID 12752 | — |
| Reactant | HCID 58094900 | HCID 58094900 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58094809 | HCID 58094809 | 31% |
Reaction Steps
A mixture of N-{7-[5-(1-allyl-1H-imidazol-2-yl)-4-(2,4-dichlorophenyl)-2-thienyl][1,3]thiazolo[5,4-d]pyrimidin-2-yl}acetamide (200.0 mg, 0.3792 mmol), acetic acid (5 mL, 90 mmol) and DCM (25 mL) was degassed with vacuum and then the atmosphere was replaced with nitrogen. To the mixture, tetrakis(triphenylphosphine)palladium(0) (10.7 mg, 0.00923 mmol) and phenylsilane (0.187 mL, 1.517 mmol) were added. The resulting mixture was stirred at 40° C. for 30 min. The mixture was allowed to cool to rt followed by adding water and DCM. After being stirred for 10 min, the organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Column chromatography was performed to yield the title compound (57.3 mg, 31%) as a pale yellow solid. LCMS: (AA) ES+ 487, 489. 1H NMR (400 MHz, d6-DMSO) δ: 12.74 (bs, 1H), 11.88 (bs, 1H), 8.95 (s, 1H), 8.52 (s, 1H), 7.77 (d, J=2.3 Hz, 1H), 7.53-7.45 (m, 2H), 7.16 (bs, 1H), 6.98 (bs, 1H), 2.24 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139589B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-aa4eec51bc48466cac8730315431a26f |
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| Source note | uspto-grants-2015_09 |
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