Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 68182975 | HCID 68182975 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68183057 | HCID 68183057 | 77.4% |
Reaction Steps
To a solution of ethyl 4-cyano-3-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-(2-naphthyl)ethyl]-5-(morpholin-4-yl)thiophene-2-carboxylate (0.126 g, 0.223 mmol) in ethanol (4.0 mL) and methylene chloride (1.0 mL) was added hydrazine (23.3 mg, 0.727 mmol). After 40 h of stirring at rt, hydrazine (25 mg, 0.78 mmol) was added and the mixture was stirred at rt for another 22 h. The mixture was filtered and concentrated. Purification on a silica gel column (continuous gradient of MeOH/DCM 0-20%) to afford a white solid product (0.0672 g, yield 77.1%). LCMS: (FA) ES+ 390. 1H NMR (400 MHz, d-chloroform) δ: 7.86-7.71 (m, 3H), 7.59 (s, 1H), 7.50-7.42 (m, 2H), 7.37 (dd, J=8.5, 1.8 Hz, 1H), 5.79 (d, J=4.0 Hz, 1H), 4.32 (d, J=3.5 Hz, 1H), 4.19-4.07 (m, 1H), 3.85-3.74 (m, 4H), 3.62 (ddd, J=12.5, 4.5, 2.3 Hz, 1H), 3.59-3.51 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765746B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ab07f7c4c01746a9889189aec4bf2eb5 |
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| Source note | uspto-grants-2014_07 |
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