Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,4-Dioxa-8-azaspiro(4.5)decane | HCID 67435 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | HCID 67282421 | HCID 67282421 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67282815 | HCID 67282815 | 77% |
Reaction Steps
Palladium acetate (8 mg, 0.038 mmol), X-Phos (18 mg, 0.038 mmol), and cesium carbonate (270 mg, 0.83 mmol) were combined in anhydrous toluene (2 mL), and nitrogen bubbled through the solution for 5 minutes. A solution of 5,7-dichloro-1-(4-methoxybenzyl)-3-(naphthalen-2-ylmethyl)-1H-benzo[e][1,4]diazepin-2(3H)-one (370 mg, 0.76 mmol) and 1,4-dioxa-8-azaspiro[4.5]decane (0.12 mL, 0.91 mmol) in toluene (2 mL) was added and then heated to 120° C. under a nitrogen blanket for 14 hours. The solution was cooled, diluted with ethyl acetate, washed with water, brine, dried with sodium sulfate, decanted, then concentrated in the presence of silica. Column chromatography eluting with a gradient of 10-70% ethyl acetate in hexanes provided 7-chloro-1-(4-methoxybenzyl)-3-(naphthalen-2-ylmethyl)-5-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-1H-benzo[e][1,4]diazepin-2(3H)-one. (345 mg, 77% yield). ESI m/z measured 596.2321 [M+H]+. calculated 596.2316.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604023B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-4c8364e39cb64e22af15dc328e54652e |
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| Source note | uspto-grants-2013_12 |
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