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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46008Generated: October 28, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 44218281, compound

https://huagongshe.com/reaction/46008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57453429HCID 57453429—
ReactantHCID 57989597HCID 57989597—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 44218281HCID 4421828158%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetic acid AC10 (0.282 mmol) in dichloromethane (10 ml/mmol) was added diisopropyl ethylamine (4 equiv.) at 0° C. followed by the addition of HOBT (1.0 equiv.) and EDCI (1.5 equiv.). The resultant solution was stirred at 25° C. for 15 min. It was again cooled to 0° C. and a solution of N-((4-(4-cyclopropyl-piperazin-1-yl)piperidin-4-yl)methyl)isonicotinamide dihydrochloride AM12 (1.2 equiv.) in DMF (2 ml) was added. The reaction mixture was stirred for 16 h at 25° C. The mixture was diluted with dichloromethane, washed with saturated ammonium chloride solution, brine, saturated sodium bicarbonate and finally again with brine. The organic layer was dried over sodium sulfate and evaporated to dryness under reduced pressure to yield the crude product which was purified by column chromatography. Yield: 58%. MS, Rt=3.2 min, m/z=731.5 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541573B2
Source datasetuspto-grants-2013_09
ORD IDord-c8424830212444c9afd62d74d99a516a
Source noteuspto-grants-2013_09