HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hydroxybenzotriazole → 3-Amino-4-bromo-N-(2-(4-methylpiperazin-1-yl)benzyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-(4-Methyl-1-piperazinyl)benzenemethanamine | HCID 2795568 | — |
| Reactant | 3-Amino-4-Bromobenzoic Acid | HCID 3418752 | — |
| Reactant | N1,N1-dimethyl-N2-((propylimino)methylene)ethane-1,2-diamine | HCID 86695678 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Amino-4-bromo-N-(2-(4-methylpiperazin-1-yl)benzyl)benzamide | HCID 86695677 | — |
Reaction Steps
N1,N1-dimethyl-N2-((propylimino)methylene)ethane-1,2-diamine (0.70 ml, 3.99 mmol) was added to a stirred solution/suspension of 3-amino-4-bromobenzoic acid (719 mg, 3.33 mmol), (2-(4-methylpiperazin-1-yl)phenyl)methanamine (820 mg, 3.99 mmol) and HOBt (140 mg, 1.0 mmol) in dry DCM (20 ml) under argon. After 24 hrs the reaction mixture was diluted with DCM and washed several times with water. The solvent was removed in vacuo and the resulting yellow oil was triturated with DCM/diethyl to give a yellow crystalline powder;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883819B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-af0775104a0a4395ada3c99c99167468 |
| Source note | uspto-grants-2014_11 |