Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68812286 | HCID 68812286 | — |
| Reactant | HCID 68812883 | HCID 68812883 | — |
| Product | HCID 57893424 | HCID 57893424 | 66% |
Reaction Steps
Ethyl 2-[(2-chlorophenyl)methyl]-5-hydroxy-3-oxo-6-phenyl-2,3-dihydro-4-pyridazinecarboxylate. Sodium hydride (0.040 g of a 60% oil suspension, 1.00 mmol) was added to a stirred solution of ethyl 5-hydroxy-3-oxo-6-phenyl-2,3-dihydro-4-pyridazinecarboxylate (example 4(b), 0.100 g, 0.384 mmol) in dimethylformamide (1.5 mL) under nitrogen. After 15 min stirring at room temperature, the mixture was cooled in an ice bath and 2-chlorobenzyl bromide (0.051 mL, 0.384 mmol) injected. The mixture was stirred for 18 h while warming to room temperature, then poured into 0.1M aqueous hydrochloric acid (50 mL) and extracted with ethyl acetate. The extracts were washed with water and brine, then dried (MgSO4), evaporated under reduced pressure and the residue chromatographed (silica gel, 1-5% methanol/dichloromethane) to give the title compound (0.098 g, 66%) as a colourless gum. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.50 (t, J=7.20 Hz, 3H) 4.55 (q, J=7.07 Hz, 2H) 5.54 (s, 2 H) 7.20-7.28 (m, 3H) 7.35-7.52 (m, 4H) 7.75-7.84 (m, 2H) 13.83 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE044613E1 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f99e8c9a733f4ea0810be5d93624cdd5 |
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| Source note | uspto-grants-2013_11 |
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