HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672291Generated: October 30, 2026
N,N'-Dimethylethylenediamine → HCID 66790319, compound
https://huagongshe.com/reaction/1672291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-2-chlorotoluene | HCID 609899 | — |
| Reactant | 7-Amino-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one | HCID 13665546 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66790319 | HCID 66790319 | 39.6% |
Reaction Steps
A mixture of 7-amino-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one (compound obtained in Reference Example 3(1); 150 mg), 5-bromo-2-chlorotoluene (321 mg), copper(I) iodide (37 mg), potassium carbonate (216 mg), N,N′-dimethylethylenediamine (40 μL) and toluene (8 mL) was heated at 110° C. overnight under argon atmosphere. After cooling, to the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel (solvent; n-hexane/ethyl acetate=4/1→1/1) to give 7-amino-4-(4-chloro -3-methylphenyl)-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one (98 mg) as a pale orange powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07998956B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-3b8072579b1a45a19f330f11e6f91cf2 |
|---|
| Source note | uspto-grants-2011_08 |
|---|