Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 69558031 | HCID 69558031 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 21034896 | HCID 21034896 | 25.3% |
Reaction Steps
To anhydrous N,N-dimethylformamide (3.46 mL, 43.5 mmol) at 0° C. was added phosphorus oxychloride (1.83 mL, 19.2 mmol) dropwise. The mixture was warmed to room temperature and stirred for 30 minutes. The mixture was cooled in an ice-bath, and 6-acetoxy-7-methoxy-1-(3-ethoxy-benzyl)-1H-isoquinoline-2-carboxylic acid ethyl ester (3.7 mg, 8.70 mmol) in dichloromethane (8 mL) was added dropwise. After addition was complete, the mixture was heated on an oil bath for 4 hrs at 80° C. The mixture was cooled to 0° C. and a solution of potassium acetate (5.26 g, 52.2 mmol) in water (10 mL) was added slowly. The mixture was then heated at 80° C. for 20 minutes. The mixture was cooled, poured into water and diluted with dichloromethane (60 mL). The organic layer was washed water (2×80 mL), saturated aqueous sodium bicarbonate solution (50 mL), saturated aqueous sodium chloride solution (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford a crude oil. Flash chromatography (Merck Silica gel 60, 70–230 mesh, 20% ethyl acetate/hexane) afforded 6-acetoxy-1-(3-ethoxy-benzyl)-4-formyl-7-methoxy-1H-isoquinoline-2-carboxylic acid ethyl ester as a colorless oil (1.0 g, 25% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067529B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-ccc5b746b658491f813e03a777362aca |
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| Source note | uspto-grants-2006_06 |
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