HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364162Generated: October 31, 2026
N,N'-Dimethylethylenediamine → HCID 16048984, compound
https://huagongshe.com/reaction/1364162
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylhydantoin | HCID 69217 | — |
| 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 16048984 | HCID 16048984 | — |
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) (80 mg, 0.23 mmol), 1-methylhydantoin (52 mg, 0.46 mmol), potassium carbonate (95 mg, 0.7 mmol), copper (I) iodide (13 mg, 0.07 mmol) and N,N′-dimethyl-1,2-ethanediamine (8 μl, 0.07 mmol) in dioxane (2 ml) was heated in the microwave (normal absorption) at 150° C. for 2 hours. The reaction mixture was purified by SCX cartridge, followed by Mass Directed Autopreparation and column chromatography on silica gel, eluting with a mixture of 2M ammonia in methanol/dichloromethane (0-5%) to afford the title compound (E38). MS (ES+) m/e 380 [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-6e07fef232094d719d7dd76e6db7b67d |
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| Source note | uspto-grants-2011_02 |
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