Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-chloro-2-methoxy-N-(5-methyl-1,3-thiazol-2-yl)benzamide | HCID 2678144 | — |
| Reactant | 4-(Chloromethyl)-1,3-thiazole | HCID 2763290 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178490689 | HCID 178490689 | 72% |
Reaction Steps
To a solution of Example 18A (2.65 g, 9.4 mmol) in N,N-dimethylformamide (20 mL) at 0° C. was added sodium hydride (60% dispersion in mineral oil, 0.247 g, 10.3 mmol). The reaction mixture was stirred for 30 min. and then treated with commercially available 4-(chloromethyl)thiazole (1.25 g, 9.4 mmol). The resulting mixture was stirred at room temperature for 18 h, poured into water (100 mL) and extracted with ethyl acetate (2×100 mL). The organics were washed with water, brine (2×100 mL), dried over MgSO4, filtered, and concentrated. The residue was purified by using an Analogix® Intelliflash280 ™ (SiO2, 0-50% ethyl acetate in hexanes) to afford the title compound (2.56 g, 72% yield). 1H NMR (300 MHz, DMSO-d6) δ ppm 2.28 (s, 3 H), 3.77 (s, 3 H), 5.50 (s, 2 H), 7.10 (d, J=8.7 Hz, 1H), 7.31 (d, J=1.6 Hz, 1 H), 7.38-7.52 (m, 2 H), 7.63 (dd, J=14.5, 2.6 Hz, 1 H), 9.09 (d, J=2.0 Hz, 1 H). MS (DCI) m/z 398 (M+H)+; MS (DCI) m/z 380 (M+H)+. Anal. Calculated for C16H14ClN3O2S2: C, 50.59; H, 3.71; N, 11.06. Found: C, 50.57; H, 3.02; N, 11.03.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-ad7f81ca1c624cc38d99d0a36598f163 |
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| Source note | uspto-grants-2012_12 |
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