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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241422Generated: October 31, 2026

Water → 4-[2-(2-amino-5-iodopyridin-3-yl)-3H-benzimidazol-5-yl]morpholin-3-one

https://huagongshe.com/reaction/241422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Amino-5-iodopyridine-3-carbaldehydeHCID 17750177—
ReactantSodium BisulfiteHCID 23665763—
Reactant4-(3,4-Diaminophenyl)morpholin-3-oneHCID 66869742—
SolventDimethylformamideHCID 6228—
Product4-[2-(2-amino-5-iodopyridin-3-yl)-3H-benzimidazol-5-yl]morpholin-3-oneHCID 66870007—

Reaction Conditions

Temperature150 °C

Reaction Steps

22.4 320 mg (1.544 mmol) of 4-(3,4-diaminophenyl)morpholin-3-one are dissolved in 4 ml of DMF, and 382.99 mg (1.544 mmol) of 2-amino-5-iodopyridine-3-carbaldehyde and 0.913 ml (4.633 mmol) of 38-40% sodium hydrogensulfite solution are added at room temperature. The mixture is stirred at 150° C. for 18 hours. The batch is cooled to room temperature, poured into 20 ml of water, the precipitate which deposits in the process is separated off and washed well with about 10 ml of water. The precipitate is triturated with about 25 ml of acetonitrile, and the undissolved crystals are separated off and dried, giving 4-[2-(2-amino-5-iodopyridin-3-yl)-3H-benzimidazol-5-yl]morpholin-3-one; HPLC-MS [M+H]+ 436.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648201B2
Source datasetuspto-grants-2014_02
ORD IDord-d3f5f62f8f054c739c70504ffeb3f729
Source noteuspto-grants-2014_02