HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585599Generated: October 30, 2026
Dimethylformamide → HCID 22337835, compound
https://huagongshe.com/reaction/585599
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Aminonaphthol | HCID 90295 | — |
| Reactant | 4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazole | HCID 9794289 | — |
| Product | HCID 22337835 | HCID 22337835 | 30% |
Reaction Steps
5-methyl-2-phenyl-4-Chloromethyloxazole (3.34 g) is added to a chilled mixture of 2-Amino-5-naphthol (2.55 g) and sodium hydride (0.65 g) in dimethylformamide (100 mL). Let stir overnight at room temperature. Concentrate in vacuo. Redilute with ethylacetate and absorb onto silica gel. Chromatograph (ethyl acetate/hexane) to give 2-amino-5-(methyl-2-phenyl-oxazol-4-ylmethoxy)naphthalene (1.59 g, 30%). Without further characterization this amine and triethylamine (0.67 mL) were dissolved in dichloromethane (75 mL). Cooled in an acetone and dry ice bath. Triflic anhydride (0.81 mL) was added and the mixture had warmed to room temperature overnight. Partition between water and ethyl acetate. Separate and dry with magnesium sulfate. Concentrate at rotovap, and triturate with ethyl acetate to provide the title compound (0.70 g, 30%) as a white solid, m.p. 192-194° C. 1H NMR (DMSO-d6, 400 MHz): δ 2.49 (s, 3H), 5.21 (s, 2H), 7.17 (d, 1H), 7.36 (d, 1H), 7.46-755 (m, 5H), 7.73 (s, 1H), 7.93-7.97 (m, 2H), 8.13 (d, 1H). MS [EI, m/z]: 462 [M]+. Anal. Calcd. for C22H17F3N2O4S 0.75(H2O): C, 55.52; H, 3.92; N, 5.89. Found: C, 55.62; H, 4.13; N, 5.45.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933322B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-233a1ef688d34c35b56e9d34235f1977 |
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| Source note | uspto-grants-2005_08 |
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