Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | D-Aspartic Acid | HCID 83887 | — |
| Reactant | 4-(4-Fluoro-3-isocyanato-benzyl)-2H-phthalazin-1-one | HCID 59856545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68978764 | HCID 68978764 | — |
Reaction Steps
To a suspension of 4-(3-isocyanato-benzyl)-2H-phthalazin-1-one (2)(1.4 g, 4.7 mmol) in dry DCM (40 ml) was added D-aspartic acid (0.455 g, 5.0 mmol), followed by triethylamine (1.4 ml, 10.0 mmol). The reaction was stirred at room temperature for 4 days. The reaction mixture was then filtered. The filtrate was then diluted with water (20 ml) and washed twice with DCM (2×20 ml). The combined DCM layers were dried over sodium sulfate and then concentrated in vacuo to afford a crude oil which was subjected to flash chromatography eluent neat ethyl acetate to remove impurity and the then 1:1 ethyl acetate/methanol to remove the desired component. (Rf of 0.2 in 1:1 ethyl acetate methanol). Single peak in LC-MS analysis, (0.79 g) requiring no further purification; m/z (LC-MS, ESP), RT=2.70 (M+H) 384;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902193B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e4cb7af33a5c4bd5a56a5f4010e4c443 |
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| Source note | uspto-grants-2011_03 |
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