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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869780Generated: October 27, 2026

2,6-Dichlorobenzaldehyde → Methyl 3-[2-(2,6-dichlorophenyl)-4-phenylsulfanyl-1,2,3,4-tetrahydroquinolin-6-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

https://huagongshe.com/reaction/1869780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DichlorobenzaldehydeHCID 6737—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantPhenyl Vinyl SulfideHCID 74572—
ReactantYtterbium triflateHCID 2733225—
ReactantMethyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoateHCID 22227788—
SolventAcetonitrile methylene chlorideHCID 21877088—
ProductMethyl 3-[2-(2,6-dichlorophenyl)-4-phenylsulfanyl-1,2,3,4-tetrahydroquinolin-6-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoateHCID 1145605481%

Reaction Steps

Methyl 3-(4-aminophenyl)-2-[(tert-butoxycarbonyl)amino]propanoate 4 (38.2 g) solubilized in a 50/50 mixture of CH3CN/CH2Cl2 is added, at room temperature, to a mixture of Yb(OTf)3 (0.05 equ.) and MgSO4 (3 equ.) in CH3CN/CH2Cl2 (50/50,400 ml). Solid 2,6-dichlorobenzaldehyde (1.1 equ.) is then added and after 2 h, phenyl vinyl sulfide (1.2 equ.) is added dropwise. After one night, insolubles are filtered and the solvents evaporated. The residue is purified by silica gel chromatography using hexane mixture/AcOEt 80/20 as eluent to give methyl 2-[(tert-butoxycarbonyl)amino]-3-[2-(2,6-dichlorophenyl)-4-(phenylsulfanyl)-1,2,3,4-tetrahydro-6-quinolinyl]propanoate 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638630B2
Source datasetuspto-grants-2009_12
ORD IDord-dfc48f339da447d6bd92e996368ca0b0
Source noteuspto-grants-2009_12