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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456618Generated: October 30, 2026

Benzyl chloroformate → HCID 136358105, compound

https://huagongshe.com/reaction/456618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 178420814HCID 178420814—
CatalystTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductHCID 136358105HCID 136358105—

Reaction Steps

Benzyl chloroformate (150 mg) (Aldrich, Milwaukee, Wis.) was added to a mixture of 3-(1H-pyrrol-2-yl)-1H-pyrazolo[3,4-b]pyridine (120 mg) (from Example 2) and triethylamine (3 drops) in dichloromethane (DCM). After stirring at room temperature for one hour, the reaction was concentrated and purified on a silica gel column to give 3-(1H-pyrrol-2-yl)-pyrazolo[3,4-b]pyridine-1-carboxylic acid benzyl ester. It was then combined with di-morpholine methane (300 mg) (Aldrich, Milwaukee, Wis.), THF (2 mL), water (0.2 mL) and acetic acid (2 drops). The mixture was heated at 90° C. for 20 hours. The reaction was concentrated and purified on a silica gel column to give 30 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186716B2
Source datasetuspto-grants-2007_03
ORD IDord-a98493c1609149d9ba87090025e41fe0
Source noteuspto-grants-2007_03