HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423374Generated: November 1, 2026
Dimethylbarbituric acid → HCID 66628105, compound
https://huagongshe.com/reaction/2423374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | HCID 66628674 | HCID 66628674 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 66628105 | HCID 66628105 | 112% |
Reaction Steps
81 mg of 1,3-dimethylbarbituric acid and 12 mg of tetrakis (triphenylphosphine) palladium were added to 190 mg of (1R,2R,3R,5R,6R)-2-allyloxycarbonylamino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 2-butyl ester 6-ethyl ester dissolved in chloroform under a nitrogen atmosphere, and the mixture was stirred for 1 hour at 50° C. The reaction solution was concentrated under reduced pressure, and the obtained residue was purified by column chromatography (silica gel: Kanto Chemical silica gel 60 (spherical), eluent: hexane-ethyl acetate=5:1), thereby yielding 180 mg of (1R,2R,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzyloxy)-6-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid 2-butyl ester 6-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07960579B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-a249d91dee754b3b941d348975739177 |
|---|
| Source note | uspto-grants-2011_06 |
|---|