HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264937Generated: October 31, 2026
Iodine chloride → 7-Fluoro-3-(2-fluoro-4-iodo-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2264937
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | 7-Fluoro-3-(2-fluoro-4-trimethylsilanyl-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester | HCID 59596472 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Fluoro-3-(2-fluoro-4-iodo-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester | HCID 59596593 | 38% |
Reaction Steps
A solution of 7-fluoro-3-(2-fluoro-4-trimethylsilanyl-phenylamino)-1H-pyrrolo[3,2-c]pyridine-2-carboxylic acid ethyl ester (500 mg, 1.28 mmol) in CH2Cl2 (15 mL) was cooled to 0-5° C. and treated dropwise with iodine monochloride solution (2.6 mL, 1M in CH2Cl2). The mixture was stirred at 0-5° C. for one hour and then quenched by addition of a saturated aqueous sodium thiosulfate solution (10 mL). The mixture was diluted with water and dichloromethane. The precipitate formed was filtered off, washed with diethyl ether and dried under vacuum at 50° C. to give the title compound as a yellow solid (218 mg, 38%). LCMS (method B): RT=2.87 min, M+H+= 444.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855216B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-ebe984b0cdaa4b0aa12744c3ae55bb48 |
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| Source note | uspto-grants-2010_12 |
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