Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 136141710 | HCID 136141710 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135774181 | HCID 135774181 | 12.5% |
Reaction Steps
To a solution of 2-Chloro-N-[2-(1-methyl-1H-pyrazol-4-yl)-6-oxo-5,6-dihydro-1H-[1,2]diazepino[4,5,6-cd]indol-8-yl]-acetamide 270(a) (100 mg, 0.28 mmol) in DMF (1.5 mL) was added Cs2CO3 (˜5 eq.) followed by benzyl amine (33 mg, 0.3 mmoL). The resulting mixture was heated at 50° C. overnight. Excess Cs2CO3 was filtered and the clear dark solution was purified by reverse phase HPLC to afford 15 mg of desired product as yellow solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132533B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-7c51d14a7a844b2fae8e3949a6a29db4 |
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| Source note | uspto-grants-2006_11 |
|---|