HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-tert-Butyl-3-((4-(2-chloro-4-(3-(cyclopropylmethyl)ureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 3-((4-(4-Amino-2-chloro-3-fluorobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide | HCID 57917628 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-Butyl-3-((4-(2-chloro-4-(3-(cyclopropylmethyl)ureido)-3-fluorobenzoyl)piperazin-1-yl)methyl)benzamide | HCID 57917615 | 193.5% |
Reaction Steps
To a stirred solution of bis(trichloromethyl) carbonate (0.076 mmol, 22.60 mg) in dichloromethane (3 mL) was added triethylamine (40 mL) and 3-((4-(4-amino-2-chloro-3-fluorobenzoyl)piperazin-1-yl)methyl)-N-tert-butylbenzamide (0.206 mmol, 92 mg) in dichloromethane (3 mL). The reaction mixture was heated to reflux for 2 hours. After this time the reaction was allowed to cool to room temperature and cyclopropylmethylamine (35 μl, 0.412 mmol) and triethylamine (35 μl) were added. After 30 minutes stirring, the volatiles were removed under reduced pressure and the crude residue was purified by silica chromatography (eluting with 5% methanol in dichloromethane) to yield the title compound (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314091B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c0e6eeff1a524151a737c7c2ce05d9d3 |
| Source note | uspto-grants-2012_11 |