HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-2-chlorophenol → 4-(2-(N-methylcarbamoyl)4-pyridyloxy)-3-chloroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-2-chlorophenol | HCID 77578 | — |
| Reactant | 4-Chloro-N-methylpicolinamide | HCID 1476814 | — |
| Product | 4-(2-(N-methylcarbamoyl)4-pyridyloxy)-3-chloroaniline | HCID 23614562 | — |
Reaction Steps
Entry 20: According to Method A1, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-N-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)-3-chloroaniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)-3-chloroaniline according to Method C1a to afford the urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124630B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-84422879372c4677a22646794fa26a40 |
| Source note | uspto-grants-2012_02 |