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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant(S)-Methyl 2-Boc-amino-3-iodopropionateHCID 11416215—
Reactant6,7-Dichloro-3-dimethylphosphonomethyl-2-bromoquinolineHCID 54046132—
CatalystPalladium ChlorideHCID 24290—
CatalystZinc copper coupleHCID 10290809—
SolventBenzeneHCID 241—
SolventDimethylacetamideHCID 31374—
Productmethyl (R)-alpha-t-butoxycarbonylamino-6,7-dichloro-3-dimethylphosphonomethyl-2-quinolinepropionateHCID 5389368063.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710139
Source datasetuspto-grants-1998_01
ORD IDord-8e3d42c3d3194c7fad4c88d391e1e112
Source noteuspto-grants-1998_01