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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41800Generated: November 4, 2026

Stannous chloride dihydrate → methyl 2-[({2'-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl}methyl)amino]-3-aminobenzoate

https://huagongshe.com/reaction/41800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactantmethyl 2-[({2'-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl}methyl)amino]-3-nitrobenzoateHCID 69916720—
SolventMethanolHCID 887—
Productmethyl 2-[({2'-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl}methyl)amino]-3-aminobenzoateHCID 6991671884.4%

Reaction Steps

A mixture of methyl 2-[({2′-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl}methyl)amino]-3-nitrobenzoate (compound 21b, 8.396 g) and tin (II) chloride dihydrate (13.56 g) in methanol (155 mL) was heated under reflux for 2 hr. The reaction mixture was concentrated under reduced pressure, and to the concentrated residue were added saturated aqueous sodium hydrogen carbonate and ethyl acetate. The mixture was stirred for 1 hr, and filtered, and the insoluble material was washed with ethyl acetate. The filtrate and washing were combined, and concentrated under reduced pressure, and the concentrated solution was extracted with ethyl acetate. The ethyl acetate solution of the resultant product was dried over magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure, and the concentrated residue was purified by silica gel column (hexane→thexane:AcOEt=5:1→4:1→3:1→2:1→3:2) to give methyl 2-[({2′-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl}methyl)amino]-3-aminobenzoate (compound 22b) (6.68 g, 84%) as a brown amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530506B2
Source datasetuspto-grants-2013_09
ORD IDord-6d2143a7f10a4486995a19065cda3944
Source noteuspto-grants-2013_09