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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070343Generated: November 3, 2026

HCID 131730050, compound → HCID 131730049, compound

https://huagongshe.com/reaction/2070343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131730050HCID 131730050—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductHCID 131730049HCID 131730049—

Reaction Steps

To (4-{2-[(4-chloro-3-nitrophenyl)amino]-1-methylbenzimidazol-5-yloxy}-(2-pyridyl))-N-methylcarboxamide in acetic acid was added Fe dust (3 eq) and stirred at ambient temperature for 16 h. The mixture was then filtered and basified with saturated sodium bicarbonate and partitioned between ethyl acetate and water. The organic layer was dried with sodium sulfate and concentrated and passed through a plug of silica to yield (4-{2-[(3-amino-4-chlorophenyl)amino]-1-methylbenzimidazol-5-yloxy}-(2-pyridyl))-N-methylcarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299108B2
Source datasetuspto-grants-2012_10
ORD IDord-f2c6df3002a74457b2f676eb3ffa5043
Source noteuspto-grants-2012_10