HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-N-(1-(5-bromo-2-((2-methoxyethyl)amino)pyrimidin-4-yl)-2-(3,5-difluorophenyl)ethyl)-2-(3-(difluoromethyl)-4,4,7,7-tetrafluoro-4,5,6,7-tetrahydro-1H-indazol-1-yl)acetamide → (S)-5-(4-(1-(2-(3-(difluoromethyl)-4,4,7,7-tetrafluoro-4,5,6,7-tetrahydro-1H-indazol-1-yl)acetamido)-2-(3,5-difluorophenyl)ethyl)-2-((2-methoxyethyl)amino)pyrimidin-5-yl)-2-fluorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-N-(1-(5-bromo-2-((2-methoxyethyl)amino)pyrimidin-4-yl)-2-(3,5-difluorophenyl)ethyl)-2-(3-(difluoromethyl)-4,4,7,7-tetrafluoro-4,5,6,7-tetrahydro-1H-indazol-1-yl)acetamide | HCID 90281357 | — |
| Reactant | (R)-5-(4-(2-(3,5-difluorophenyl)-1-(2-(3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl)acetamido)ethyl)-2-((2-methoxyethyl)amino)pyrimidin-5-yl)-2-fluorobenzamide | HCID 90290144 | — |
| Product | (S)-5-(4-(1-(2-(3-(difluoromethyl)-4,4,7,7-tetrafluoro-4,5,6,7-tetrahydro-1H-indazol-1-yl)acetamido)-2-(3,5-difluorophenyl)ethyl)-2-((2-methoxyethyl)amino)pyrimidin-5-yl)-2-fluorobenzamide | HCID 90281525 | — |
Reaction Steps
The title compound (12E) was prepared according to the method presented for the synthesis of compound 11J of Example 11 utilizing 12D. 1H NMR (400 MHz, CD3OD) δ 8.80 (d, J=8.0 Hz, 1H), 8.05 (s, 1H), 7.47-7.29 (m, 2H), 7.21 (dd, J=10.7, 8.6 Hz, 1H), 6.97-6.61 (m, 2H), 6.44 (d, J=6.1 Hz, 2H), 5.22 (dd, J=14.9, 7.7 Hz, 1H), 5.05 (s, 2H), 3.89-3.51 (m, 4H), 3.41 (s, 3H), 3.02 (ddd, J=20.2, 13.2, 7.5 Hz, 2H), 2.66-2.28 (m, 4H). MS (m/z) 730.24 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09050344B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-c72e3deb4ba543438e2771d9ed396df5 |
| Source note | uspto-grants-2015_06 |