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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888236Generated: November 1, 2026

Hydrazine → HCID 178511483, compound

https://huagongshe.com/reaction/1888236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2,5-Dioxo-pyrrolidin-1-yl)-ethanesulfonyl chlorideHCID 18524013—
Reactant5-phenyl-3-(4-piperidinyl)-1H-indazole-7-carboxamide hydrochlorideHCID 178479539—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 178511483HCID 17851148317%

Reaction Steps

To a solution of 5-phenyl-3-(4-piperidinyl)-1H-indazole-7-carboxamide hydrochloride (Example 2) (50 mg, 0.14 mmol) in DMF (3 mL) was added diisopropylethylamine (100 uL, 0.56 mmol), DMAP (25 mg, 0.014 mmol) and 2-(2,5-dioxo-1-pyrrolidinyl)ethanesulfonyl chloride (53 mg, 0.168 mmol). After the reaction mixture was stirred at room temperature overnight, hydrazine (4 eq) was added. The reaction mixture was stirred for 4 hrs. The solution was filtered. The filtrate was concentrated and the residue was purified by using a Gilson semi-preparative HPLC system, eluting with 10% B to 80% B, where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% trifluoroacetic acid) pumped at 25 mL/min to afford the title compound (10 mg, 17%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501780B2
Source datasetuspto-grants-2013_08
ORD IDord-7ec8e608db3b4f5792ff7387d5ac8456
Source noteuspto-grants-2013_08