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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506164Generated: November 3, 2026

1-Methylpiperazine → HCID 24865996, compound

https://huagongshe.com/reaction/506164

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 24864896HCID 24864896—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 24865996HCID 2486599653%

Reaction Steps

To 5-[3-(5-formyl-2-thienyl)phenyl]-4-(1H-indol-5-ylamino)nicotinonitrile 150 (100 mg, 0.238 mmol) in CH2Cl2 (5 mL) and NMP (0.5 mL), cooled with ice-water bath, was added Na(OAc)3BH (264 mg, 1.2 mmol) and N-methylpiperazine (133 μL, 1.2 mmol). The resulting mixture was stirred at r.t. overnight and partitioned between CH2Cl2 and aq. NaHCO3. The combined organics were dried over Na2SO4, concentrated and purified by preparative TLC eluting with 10% MeOH/CH2Cl2 to give 63 mg (53% yield) of the title compound as a light yellow solid. MS: 505.2 (M+H); melting range: 120-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781591B2
Source datasetuspto-grants-2010_08
ORD IDord-048fa6b3170549bf82813e0013222715
Source noteuspto-grants-2010_08