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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372408Generated: October 31, 2026

Water → HCID 22571064, compound

https://huagongshe.com/reaction/1372408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrrolidineHCID 31268—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 68791479HCID 68791479—
SolventDichloromethaneHCID 6344—
ProductHCID 22571064HCID 2257106496%

Reaction Steps

To a suspension of 10 g of 3-(4-oxo-4,5,6,7,tetrahydro-1H-indol-3-yl-propionic acid (48 mmol) in 60 mL of dichloromethane was added 9.3 g (57.6 mmol) of carbonyldiimidazole. After stirring at room temperature for 2 hours, 12 mL (144 mmol) of pyrrolidine was added. The dark red reaction mixture was then stirred at room temperature overnight. The reaction was poured into water and the organic layer washed with brine, dried and concentrated to give 3-(3-oxo-3-pyrrolidin-1-yl-propyl)-1,5,6,7-tetrahydro-indol-4-one (12 g, 96% yield). 1H-NMR (300 MHz, dimethylsulfoxide-d6) δ 11.05 (br s, 1H, NH), 6.46 (d, 1H), 3.35 (m, 2H, CH2), 2.24 (m, 2H, CH2), 2.66–2.73 (m, 4H, 2×CH2), 2.44 (m, 2H, CH2), 2.26 (m, 2H, CH2), 1.96 (m, 2H, CH2), 1.82 (m, 2H, CH2), 1.73 (m, 2H, CH2). MS m/z 260 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157577B2
Source datasetuspto-grants-2007_01
ORD IDord-b69a279b5dd546ae8cc890c8bfe263b6
Source noteuspto-grants-2007_01