HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642543Generated: October 26, 2026
Trifluoroacetic acid → 2,3-Dibromo-1-(3,4-difluoro-benzyl)-4-hydroxy-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/642543
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium t-amylate | HCID 23683543 | — |
| Reactant | 4,5-dibromo-2-[(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-1-(4-fluoro-benzyl)-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 68426263 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,3-Dibromo-1-(3,4-difluoro-benzyl)-4-hydroxy-1H-pyrrolo[2,3-c]pyridine-5-carboxylic acid ethyl ester | HCID 68428317 | — |
Reaction Steps
To an ice/water bath cooled crude 4,5-dibromo-2-[(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-1-(4-fluoro-benzyl)-1H-pyrrole-3-carboxylic acid ethyl ester (29.49 g) in toluene (100 mL) was added a 25% (weight) concentration of potassium tert-pentoxide in toluene (67.04 mL) during a course of ˜5 min; after that, the reaction was stirred for 1 h in the cold bath and then poured to a stirring mixture of ice/water and ammonium chloride, organic phase was separated and washed with water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, concentrated to give the cyclized intermediate. The intermediate was then dissolved in 50 mL toluene and 50 mL TFA and stirred at room temperature for 1 h, then concentrated, the residue was partitioned between toluene and water; the organic phase was washed once with saturated sodium hydrogen carbonate, saturated sodium chloride solution respectively, then dried over anhydrous sodium sulfate, filtered, and air bubbled through the filtrate for a period of overnight. The precipitates were collected as the first crop of the title product (8.161 g). The filtrate was concentrated and purified with column directly to give the second crop of the title product (4.98 g). The title compound, ESI MS (m/z): 489 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696223B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6ae2aae8fe45453ca8c1ca5361e5a275 |
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| Source note | uspto-grants-2010_04 |
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