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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380840Generated: October 31, 2026

Iodine → HCID 59320162, compound

https://huagongshe.com/reaction/2380840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 91231834HCID 91231834—
SolventTetrahydrofuranHCID 8028—
SolventAmmonia chlorideHCID 20976574—
SolventSodium BisulfiteHCID 23665763—
ProductHCID 59320162HCID 5932016253%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of tert-butyl [1-(6,8-difluoro[1,2,4]triazolo[4,3-a]pyridin-3-yl)-1-methylethyl]carbamate (1.32 g, 4.23 mmol) in tetrahydrofuran (20 mL) under argon atmosphere and at −78° C. was slowly added LiHMDS (1M in hexanes, 9.3 mL, 9.3 mmol). It was stirred at −78° C. for 45 min, afterwards a solution of iodine (1.13 g, 4.44 mmol) in tetrahydrofuran (10 mL) was added dropwise. The resulting mixture was stirred at −78° C. for 2 hours, warmed to 0° C. and diluted with aqueous sodium bisulphite (10 mL) and saturated ammonia chloride (10 mL). It was warmed to room temperature, extracted with ethyl acetate, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude was purified by silica flash chromatography eluting with hexanes/ethyl acetate, using a gradient from 50% to 83% of ethyl acetate to yield the title compound (0.979 g, 53%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258122B2
Source datasetuspto-grants-2012_09
ORD IDord-68165f9aa47a409caca2147eafe93aed
Source noteuspto-grants-2012_09