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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026837Generated: November 4, 2026

4-[[2-[5-[[Boc(2-methoxyethyl)amino]methyl]-2-pyridyl]-7-thieno[3,2-b]pyridyl]oxy]-3-fluoroaniline → HCID 67048207, compound

https://huagongshe.com/reaction/1026837

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[[2-[5-[[Boc(2-methoxyethyl)amino]methyl]-2-pyridyl]-7-thieno[3,2-b]pyridyl]oxy]-3-fluoroanilineHCID 57919472—
ReactantHCID 58207628HCID 58207628—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 67048207HCID 6704820755%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of the amine 126 (500 mg, 0.953 mmol) in DME (4 ml) was added the carbamate 374 (460 mg, 2.5 eq, 2.383 mmol) and the reaction mixture was heated to 120° C. for 1 day. The mixture was cooled to RT, diluted with EtOAc and water and the organic phase was collected, dried over Na2SO4, filtered and concentrated. Purification of the residue by column chromatography (eluent EtOAc to 50% Acetone in EtOAc) afforded 375 as a brown oil (130 mg, 55%). MS (m/z)=672.5 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729268B2
Source datasetuspto-grants-2014_05
ORD IDord-adadecf16cc74405af1edf8cd10beac6
Source noteuspto-grants-2014_05