Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788004Generated: November 2, 2026

Hydrochloric Acid → HCID 66750308, compound

https://huagongshe.com/reaction/1788004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 57437985HCID 57437985—
SolventDichloromethaneHCID 6344—
ProductHCID 66750308HCID 6675030879.6%

Reaction Steps

To a suspension of 32.26 g (0.115 mol) of 2-(5-hydroxy-1H-indazol-3-yl)-1H-isoindole-1,3(2H)-dione in 320 ml of dichloromethane, a solution of 43.54 g (0.288 mol) of TBDMS chloride in 150 ml of dichloromethane was added. The resulting mixture was treated dropwise with 35.5 ml (0.23 mol) of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) at room temperature, obtaining a clear solution. After 3 hours the reaction mixture was poured in 300 ml of a solution 0.1 N of hydrochloric acid. The aqueous layer was separated and extracted with 200 ml of dichloromethane. Organic extracts were dried over sodium sulfate and the solvent evaporated under vacuum. The raw product was purified by flash chromatography over silica gel eluiting with dichloromethane-cyclohexane-ethyl acetate (4:4:2). 36.03 g of product as white solid were obtained. Yield=79.2%. mp=225-228° C. HPLC r.t. 8.3 [M+H]+=394 [2M+H]+=787

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511136B2
Source datasetuspto-grants-2009_03
ORD IDord-39d7897e17fc4837875fe505c7715078
Source noteuspto-grants-2009_03