HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500711Generated: October 27, 2026
Lithium Hexamethyldisilazide → 5-(2-Fluoro-4-iodophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid (2-vinyloxyethoxy)-amide
https://huagongshe.com/reaction/1500711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | O-(2-(Vinyloxy)ethyl)hydroxylamine | HCID 21867017 | — |
| Reactant | 5-(2-Fluoro-4-iodophenylamino)imidazo[1,5-a]pyridine-6-carboxylic acid methyl ester | HCID 59140136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-Fluoro-4-iodophenylamino)-imidazo[1,5-a]pyridine-6-carboxylic acid (2-vinyloxyethoxy)-amide | HCID 59140166 | 60.5% |
Reaction Steps
To a mechanically stirred solution of 5-(2-fluoro-4-iodophenylamino)imidazo[1,5-a]pyridine-6-carboxylic acid methyl ester (82.17 g, 0.2 mol) and O-(2-vinyloxyethyl)hydroxylamine (40.73 g, 0.382 mol) in dry THF (1.27 L) at 5° C. under N2 atmosphere, was added lithium bis(trimethylsilyl)amide as a solution in THF (1 L, 1 M, 1 mol) over 1 hr, maintaining the temperature below 10° C. The reaction mixture was stirred at 0-5° C. for 20 minutes before being quenched with addition water (200 ml) and saturated saline (350 mL). Volatile solvents were removed in vacuo and the residue diluted with water (1.5 L) and extracted 2-methyl tetrahydrofuran (3×1 L). The organic layers were washed water (500 mL), saturated saline (500 mL), dried (Na2CO3) and absorbed onto silica gel (200 g) and purified on silica gel (400 g) using ethyl acetate as eluent. The resultant crude product was triturated with tert-butyl methyl ether (400 mL) to yield the title compound as a brown solid (58.36 g, 60%). LCMS (Method B): RT=2.79 min, [M+H]+=483.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206174B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2b47bcc6cade45faa18c40aa82f0de66 |
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| Source note | uspto-grants-2015_12 |
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