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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62021Generated: October 28, 2026

3,4-Bis(benzyloxy)-5-nitrobenzoic acid → [(Z)-[amino-[2-(trifluoromethyl)-3-pyridinyl]methylidene]amino] 3-nitro-4,5-bis(phenylmethoxy)benzoate

https://huagongshe.com/reaction/62021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Bis(benzyloxy)-5-nitrobenzoic acidHCID 46201925—
ReactantHCID 83401048HCID 83401048—
SolventDimethylformamideHCID 6228—
Product[(Z)-[amino-[2-(trifluoromethyl)-3-pyridinyl]methylidene]amino] 3-nitro-4,5-bis(phenylmethoxy)benzoateHCID 87544316—

Reaction Steps

To a stirred solution of 3,4-bis(benzyloxy)-5-nitrobenzoic acid (0.759 g, 2 mmol) in dimethylformamide (10 mL) at room temperature was added 1,1-carbonyldiimidazole (0.34 g, 2.10 mmol) in one portion. The resulting yellow mixture was allowed to stir for ninety minutes whereupon (Z)—N′-hydroxy-2-(trifluoromethyl)nicotinimidamide (0.41 g, 2 mmol) was added in one portion. The resulting mixture was stifled at room temperature for two hours and then poured onto water (100 mL). The resulting precipitate was filtered off, washed with water and dried. After recrystallisation from dichloromethane/isopropanol, (Z)—N′-(3,4-bis(benzyloxy)-5-nitrobenzoyloxy)-2-(trifluoromethyl)nicotinimidamide was obtained as a light yellow solid, 0.88 g (78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446012B2
Source datasetuspto-grants-2016_09
ORD IDord-bfc8d16801ea486c94860d5c14b24560
Source noteuspto-grants-2016_09