HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076191Generated: October 30, 2026
Iodine chloride → 3-(2-Fluoro-4-iodo-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/2076191
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | HCID 59140179 | HCID 59140179 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Fluoro-4-iodo-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester | HCID 59140139 | 99% |
Reaction Steps
To a cold (0° C.) solution of 3-(2-fluoro-4-trimethylsilanyl-phenylamino)-5-formylaminomethyl-pyrazine-2-carboxylic acid methyl ester (480 mg, 1.28 mmol) in dichloromethane (13 mL) under N2 was added dropwise a solution of 1M iodine monochloride in dichloromethane (3.0 mL, 3.0 mmol, 2.4 eq), and the mixture was stirred at 0° C. for 1.5 hour. The reaction was quenched by addition of a saturated aqueous solution of sodium thiosulfate (3 mL). After stirring for 10 minutes the reaction mixture was poured into ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate, water and brine, dried (Na2SO4), filtered and evaporated in vacuo to afford the desired product as a yellow solid (548 mg, 99%). LCMS (method C): RT=2.65 min, [M+H]+=431.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923456B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-4769eec31504481ab033884dc728e070 |
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| Source note | uspto-grants-2011_04 |
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