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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-5-iodopyridine-3-carbaldehyde | HCID 17750177 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 4-(3,4-Diaminophenyl)morpholin-3-one | HCID 66869742 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(2-amino-5-iodopyridin-3-yl)-3H-benzimidazol-5-yl]morpholin-3-one | HCID 66870007 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648201B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-d3f5f62f8f054c739c70504ffeb3f729 |
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| Source note | uspto-grants-2014_02 |
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