HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Methyl 6-chloro-3-(2,6-dioxo-4-(trifluoromethyl)-2,3-dihydropyrimidin-1(6H)-yl)-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 6-chloro-3-isocyanato-2-methylbenzoate | HCID 21710153 | — |
| Reactant | 3-Amino-4,4,4-trifluoro-2-butenoate | HCID 73446983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 6-chloro-3-(2,6-dioxo-4-(trifluoromethyl)-2,3-dihydropyrimidin-1(6H)-yl)-2-methylbenzoate | HCID 21710140 | 58.9% |
Reaction Steps
This compound was prepared in a manner analogous to the second part of Step D, Example 1. Here, 16.7 grams (0.074 mole) of methyl 6-chloro-3-isocyanato-2-methylbenzoate was combined with 4.4 grams (0.110 mole) of 60% sodium hydride and 14.2 grams (0.076 mole) of 3-amino-4,4,4-trifluoro-2-butenoate in 600 mL of THF. The reaction product was purified by column chromatography on silica using a 1:1 mixture of EtOAc and hexane as eluant. The fractions containing product were combined and concentrated under reduced pressure, yielding 15.8 grams of subject compound. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277847B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-16ad04a994b54b608241912aceb911c0 |
| Source note | uspto-grants-2001_08 |