HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → N-[4-(N-methyl-N-pyridin-4-yl-amino)phenyl]-2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 4-(N-methyl-N-pyridin-4-yl-amino)phenylamine | HCID 23023092 | — |
| Reactant | (4-Chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 131727716 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[4-(N-methyl-N-pyridin-4-yl-amino)phenyl]-2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxamide | HCID 11670720 | 51.4% |
Reaction Steps
To a solution of 2N-(4-chlorophenylaminocarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (63 mg, 0.19 mmol) and 4-(N-methyl-N-pyridin-4-yl-amino)phenylamine (47 mg, 0.24 mmol) in DMF (3 mL), EDC (80 mg, 0.42 mmol) was added. The reaction mixture was stirred at room temperature overnight. It was then concentrated in vacuo. The residue was purified by HPLC to give the titled compound as a white powder (25 mg). MS 512.2 and 514.2 (M+H, Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612089B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-c8a2deab50d245f4a5af079ec5451393 |
| Source note | uspto-grants-2009_11 |