HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726646Generated: October 30, 2026
Water → methyl (R)-alpha-t-butoxycarbonylamino-6,7-dichloro-3-dimethylphosphonomethyl-2-quinolinepropionate
https://huagongshe.com/reaction/726646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | (S)-Methyl 2-Boc-amino-3-iodopropionate | HCID 11416215 | — |
| Reactant | 6,7-Dichloro-3-dimethylphosphonomethyl-2-bromoquinoline | HCID 54046132 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Catalyst | Zinc copper couple | HCID 10290809 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | methyl (R)-alpha-t-butoxycarbonylamino-6,7-dichloro-3-dimethylphosphonomethyl-2-quinolinepropionate | HCID 53893680 | 63.3% |
Reaction Steps
A solution of N-t-butoxycarbonyl-3-iodo-D-alanine methyl ester (0.66 g, 2 mmol) in dry benzene (3 ml) and dry dimethylacetamide (0.5 ml) was added to a zinc-copper couple (0.31 g). The resulted mixture was sonicated at 40°-45° C. under nitrogen for 2.5-3 h until no starting material remained (as judged by TLC). Tri-o-tolylphosphine (0.06 g, 0.2 mmol) and palladium chloride (0.02 g, 0.1 mmol) were added followed by a solution of 6,7-dichloro-3-dimethylphosphonomethyl-2-bromoquinoline (0.4 g, 1 mmol) in dry benzene (3 ml) and dry dimethylacetamide (0.5 ml). The resulted mixture was stirred under nitrogen at 50°-60° C. for 2.5-3 h and then allowed to cool. Water was added and the mixture was filtered through Celite, the latter was washed with ethyl acetate. The combined organic phases were separated, dried, (MgSO4) and concentrated in vacuo. The residue was coevaporated several times with toluene to remove most of the dimethylacetamide and then purified on a silica gel column using 0-2% methanol in chloroform as eluent to give 0.33 g of methyl (R)-α-t-butoxycarbonylamino-6,7-dichloro-3-dimethylphosphonomethyl-2-quinolinepropionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05710139 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-8e3d42c3d3194c7fad4c88d391e1e112 |
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| Source note | uspto-grants-1998_01 |
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