HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Chlorophenylamino)-3-methylbutanoic acid → (6-Benzoyl2-pyridyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Chlorophenylamino)-3-methylbutanoic acid | HCID 13796079 | — |
| Reactant | 2-(2-Fluoro-4-trifluoromethylphenylamino)-3-methylbutanoic acid | HCID 20283983 | — |
| Reactant | (6-Benzoyl-2-pyridyl)methanol | HCID 20293448 | — |
| Product | (6-Benzoyl2-pyridyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate | HCID 23337850 | — |
| Product | (6-Benzoyl-2-pyridyl)methyl 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoate | HCID 23337857 | — |
Reaction Steps
Following the procedure of Example 1, the acid chloride of each of 2-(4-chlorophenylamino)-3-methylbutanoic acid and 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoic acid is reacted with (6-benzoyl-2-pyridyl)methanol to yield (6-benzoyl2-pyridyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate and (6-benzoyl-2-pyridyl)methyl 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226872 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-f15f905f7005478ba8ac4a686340aa82 |
| Source note | uspto-grants-1980_10 |