HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate → 3-[({4-[(cyclohexyl{3-ethyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazol-4-yl}methyl)amino]phenyl}carbonyl)(methyl)amino]propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate | HCID 46941342 | — |
| Reactant | cyclohexyl{3-ethyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazol-4-yl}methanol | HCID 66778762 | — |
| Product | 3-[({4-[(cyclohexyl{3-ethyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazol-4-yl}methyl)amino]phenyl}carbonyl)(methyl)amino]propanoic acid | HCID 66778079 | 41% |
Reaction Steps
Using cyclohexyl{3-ethyl-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazol-4-yl}methanol (0.55 g) synthesized in Example 3(3) and ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate (0.39 g) synthesized in Example 2(2) and in the same manner as in Example 1(7), the title object compound (0.35 g, 41%) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-655a8c83b3ba4fb78caa24162e8d635a |
| Source note | uspto-grants-2013_05 |