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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931177Generated: November 3, 2026

Trityl chloride → HCID 178492069, compound

https://huagongshe.com/reaction/1931177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantHCID 10203446HCID 10203446—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
ProductHCID 178492069HCID 1784920699%

Reaction Conditions

Temperature105 °C

Reaction Steps

To 1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxo-1(2H)-pyridinyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carbonitrile (0.1 g, 0.23 mmol) in DMF (2 mL) was added NaN3 (19 mg, 0.29 mmol) and NH4Cl (21 mg, 0.38 mmol) and the reaction was heated to 105° C. for 24 h. The reaction was cooled, water (1 mL) was added, and the resulting solid filtered off and dried. The solid was placed in DMF (1 mL) and trityl chloride (60 mg, 0.2 mmol) and pyridine (0.2 mL) were added and stirred for 24 h. The reaction was quenched with water, extracted with EtOAc, and dried (Na2SO4). Purification on silica gel was not successful. The trityl group was removed with TFA (0.5 mL) in CH2Cl2 for 2 h. The solvents were removed and the compound was purified by HPLC and freeze-dried to afford 10 mg (9%) of a white solid; High Resolution Mass Spec (M+H)+ for C25H21N8O3 481.1749.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188120B2
Source datasetuspto-grants-2012_05
ORD IDord-b9d4aaa691134db391fad79b6c8a26f5
Source noteuspto-grants-2012_05