HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl acetoacetate → 4-oleamidoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Diethylenetriamine | HCID 8111 | — |
| Reactant | Oleic Acid | HCID 445639 | — |
| Product | 4-oleamidoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one | HCID 86738548 | — |
Reaction Steps
Into an apparatus similar to that in Example 1, were charged 103.1 g (1 mole) of diethylenetriamine and 116.1 g (1 mole) of methyl acetoacetate. At 110° to 120° C. and under a reduced pressure of 70 mmHg, 18 g of water and 32 g of methanol were distilled off. Then, with the addition of 282.5 g (1 mole) of oleic acid, the amide formation was effected at 210° to 215° C. to distil off 18 g of water and to obtain 4-oleamidoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04346087 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-1d41e52024264bd480439c42fcb709ca |
| Source note | uspto-grants-1982_08 |