HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364161Generated: October 31, 2026
N,N'-Dimethylethylenediamine → HCID 16048916, compound
https://huagongshe.com/reaction/1364161
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Oxazolidinone | HCID 73949 | — |
| Reactant | HCID 16048914 | HCID 16048914 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 16048916 | HCID 16048916 | — |
Reaction Steps
A mixture of 2-(4-bromophenyl)-6-cyclobutyl-2,4,5,6,7,8-hexahydropyrazolo[3,4-d]azepine (may be prepared as described in Example 35) (42 mg, 0.12 mmol), 2-oxazolidinone (21 mg, 0.24 mmol), potassium carbonate (50 mg, 0.36 mmol), copper (I) iodide (8.0 mg, 0.04 mmol) and N,N′-dimethyl-1,2-ethanediamine (5 μl, 0.04 mmol) in dioxane (1.5 ml) was heated in the microwave (high absorption) at 100° C. for 30 minutes. The same amounts again of 2-oxazolidinone, potassium carbonate, copper (I) iodide and N,N′-dimethyl-1,2-ethanediamine were added and the mixture heated in the microwave at 150° C. for 4 hours. The reaction mixture was evaporated in vacuo, then purified by SCX cartridge, followed by Mass Directed Autopreparation to afford the title compound (E37). MS (ES+) m/e 353 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888347B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-26bfdf43fed34ae7a875fabb7e48888e |
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| Source note | uspto-grants-2011_02 |
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