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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247005Generated: October 23, 2026

Benzyl chloroformate → Benzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamate

https://huagongshe.com/en/reaction/1247005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantAL-34662HCID 135453290—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl (S)-2-(6-hydroxy-1H-indazol-1-yl)-1-methylethylcarbamateHCID 13548732878%

Reaction Steps

1-((S)-2-Aminopropyl)-1H-indazol-6-ol [prepared in accordance with commonly owned WO 02/098862A1, the contents of which are by this reference incorporated herein] (2.00 g, 10.5 mmol) was suspended in THF (20 mL) and saturated aqueous sodium bicarbonate (10 mL) and benzyl chloroformate (1.50 mL, 15 mol) were added. The mixture was stirred at room temperature until the starting amine dissolved. Saturated aqueous sodium bicarbonate (150 mL) was added and the reaction mixture extracted with ethyl acetate (3×150 mL). The combined organic layers were dried (magnesium sulfate), filtered, and evaporated to give a tan foam (2.65 g, 78%) which was pure by LC/MS (+APCI) m/z 326 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129257B1
Source datasetuspto-grants-2006_10
ORD IDord-b0c0d8205a8f41f98ec32ad4ca9de451
Source noteuspto-grants-2006_10