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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334025Generated: October 31, 2026

Diisopropylethylamine → 3-(1-Cyclopropyl-isoquinoline-3-carbonyl)-2,2-dimethyl-piperazine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/334025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant2,2-Dimethyl-piperazine-1-carboxylic acid benzyl ester trifluoroacetateHCID 86688243—
Reactant1-Cyclopropyl-isoquinoline-3-carboxylic acidHCID 86688255—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(1-Cyclopropyl-isoquinoline-3-carbonyl)-2,2-dimethyl-piperazine-1-carboxylic acid benzyl esterHCID 86688256—

Reaction Steps

230 mg (1.08 mmol) 1-cyclopropyl-isoquinoline-3-carboxylic acid and 391 mg (1.08 mmol) 2,2-dimethyl-piperazine-1-carboxylic acid benzyl ester trifluoroacetate was stirred with 385 mg (1.20 mmol) TBTU and 640 μL (3.70 mmol) DIPEA in 3 mL DMF at RT for 1 h. The mixture was worked up by adding water, followed by extraction with EtOAc. Then the reaction mixture was washed with saturated aqueous NaHCO3 solution. The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. Yield: 600 mg (99%), purity: 80%; ESI-MS: m/z=444 (M+H)+; Rt(HPLC): 1.42 min (method 5)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883789B2
Source datasetuspto-grants-2014_11
ORD IDord-a3d409b280a9430ea0d83a2052ed9e82
Source noteuspto-grants-2014_11