HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylhomopiperazine → 1-[2-(2-Imidazolylmethyl)phenylcarbamoyl]-4-methylhomopiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | 11H-imidazo[1,2-c][1,3]benzodiazepin-5(6H)-one | HCID 13344922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(2-Imidazolylmethyl)phenylcarbamoyl]-4-methylhomopiperazine | HCID 13344923 | — |
Reaction Steps
To a suspension of 0.76 g of 11H-imidazo[1,2-c][1,3]benzodiazepin-5-(6H)-one in 9 ml of methylene chloride is added at once 0.41 g of N-methylhomopiperazine and the mixture is stirred at room temperature for 24 hours. The reaction mixture is filtered and the filtrate is evaporated to dryness. Recrystallization of the residue from methylene chloride-ether gave 1-[2-(2-imidazolylmethyl)phenylcarbamoyl]-4-methylhomopiperazine, the compound of formula VI wherein R1, R2, R4 -R7 are hydrogen, CnH2n is (CH2)3, R3 is methyl and Z is oxygen, melting at 139°-143°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507311 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-d08fd3aa1ae743069cc9f84fbaa6e457 |
| Source note | uspto-grants-1985_03 |