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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244071Generated: October 25, 2026

1,3-Cyclohexanedione, 2-acetyl-5,5-dimethyl- → 1-(1-Amino-4-bromo-isoquinolin-6-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indazol-4-one

https://huagongshe.com/reaction/2244071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Cyclohexanedione, 2-acetyl-5,5-dimethyl-HCID 519448—
Reactant4-Bromo-6-hydrazino-isoquinolin-1-ylamineHCID 25059692—
SolventAcetic acid ethanolHCID 18476134—
Product1-(1-Amino-4-bromo-isoquinolin-6-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indazol-4-oneHCID 2506098080.6%

Reaction Steps

A suspension of 4-Bromo-6-hydrazino-isoquinolin-1-ylamine (0.097 g, 0.38 mmol) and 2-acetyl-5,5-dimethyl-1,3-cyclohexanedione (0.074 g, 0.41 mmol) in EtOH/Acetic acid (3:1, 7 mL) is microwaved at 150° C. for 20 min. The solvent is evaporated and the residue is dried under vacuum. Purification of the crude material using a Biotage column (0-10% MeOH/CH2Cl2) afforded 0.1223 g (80%) of 1-(1-Amino-4-bromo-isoquinolin-6-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indazol-4-one. LC/MS m/z=400 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678803B2
Source datasetuspto-grants-2010_03
ORD IDord-1f050a28e0a14f89aa1c7243a6673f58
Source noteuspto-grants-2010_03