HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-methyl-N-(5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-malonamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 7-Amino-5-methyl-5H-dibenzo[b,d]azepin-6(7H)-one | HCID 10198626 | — |
| Reactant | 3-(Tert-butoxy)-2-methyl-3-oxopropanoic acid | HCID 17851702 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methyl-N-(5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-malonamic acid tert-butyl ester | HCID 69039766 | — |
Reaction Steps
To a cooled solution (0° C.) of 2-methyl-malonic acid mono-tert-butyl ester (1.01 g, 5.79 mmol) and 7-amino-5-methyl-5H,7H-dibenzo[b,d]azepin-6-one (1.15 g, 4.83 mmol) in THF (8 ml) was added hydroxybenzotriazole (652 mg, 4.83 mmol), diisopropylethylamine (624 mg, 4.83 mmol)and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (925 mg, 4.83 mmol), and the mixture was stirred overnight at r.t. The solvent was evaporated, the residue was taken up in ethyl acetate, washed with water, and dried (Na2SO4). After evaporation of the solvent, the title compound, MS: m/e=395.3 (M+H+), (920 mg, 48%) was obtained by chromatographic purification of the residue (silica gel, MeOH, CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375099B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-2a2568255a924934a7d158f5823a28b0 |
| Source note | uspto-grants-2008_05 |