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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418327Generated: October 30, 2026

1,2-Dichloroethane → Formate

https://huagongshe.com/reaction/418327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-amino-N,N-dimethylbenzylamineHCID 99294—
Reactant3-[(3,4-Dimethoxy-benzoylamino)-methyl]-benzoic acidHCID 44819543—
SolventDimethylformamideHCID 6228—
ProductFormateHCID 2831,399.3%
ProductN-[3-(3-dimethylaminomethyl-phenylcarbamoyl)-benzyl]-3,4-dimethoxy-benzamideHCID 25054030—

Reaction Steps

3-[(3,4-Dimethoxy-benzoylamino)-methyl]-benzoic acid (40 mg, 0.127 mmol), prepared as described in Example 8, was combined with EDC (38.3 mg, 0.2 mmol) and HOBt (24.3 mg, 0.18 mmol) in a reaction vial, and DMF (1 mL) was added followed by N-methylmorpholine (0.025 mL, 0.22 mmol). The resulting mixture was agitated for 1 h, then 3-dimethylaminomethyl-phenylamine (25.5 mg, 0.17 mmol) was added as a solution in DMF (0.5 mL), and the resulting mixture was agitated overnight. The product was purified directly by preparative HPLC using an acetonitrile/water/formic acid gradient providing the title compound as a formate salt (40 mg, 70% yield), MS analysis electrospray, 448 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093266B2
Source datasetuspto-grants-2012_01
ORD IDord-78ba5dfa3fb841de96e969a04a7d9213
Source noteuspto-grants-2012_01