HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Chlorophenylamino)-3-methylbutanoic acid → (2,4-Dioxo-5-methyl-1-n-propyl-3-imidazolidinyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Chlorophenylamino)-3-methylbutanoic acid | HCID 13796079 | — |
| Reactant | (2,4-Dioxo-5-methyl-1-n-propyl-3-imidazolidinyl)methanol | HCID 20342644 | — |
| Product | (2,4-Dioxo-5-methyl-1-n-propyl-3-imidazolidinyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate | HCID 20342663 | — |
Reaction Steps
Using the procedure of Example 1, (2,4-dioxo-5-methyl-1-n-propyl-3-imidazolidinyl)methanol is reacted with the acid chloride of 2-(4-chlorophenylamino)-3-methylbutanoic acid to give (2,4-dioxo-5-methyl-1-n-propyl-3-imidazolidinyl)methyl 2-(4-chlorophenylamino)-3-methylbutanoate (A'; R is carbonyl, R' is ethylidene, R1 =R4 =R5 is hydrogen, R2 is p-chlorophenyl, R3 is isopropyl, R6 is n-propyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04200758 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-56eae6cd0f4246cca46a531a56232468 |
| Source note | uspto-grants-1980_04 |