Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362935Generated: October 29, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3,4-Dichlorobenzoic acid N'-(5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carbonyl)hydrazide

https://huagongshe.com/reaction/1362935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3,4-DichlorobenzhydrazideHCID 311996—
Reactant5-chloro-1H-pyrrolo(3,2-b)pyridine-2-carboxylic acidHCID 11665585—
SolventDimethylformamideHCID 6228—
Product3,4-Dichlorobenzoic acid N'-(5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carbonyl)hydrazideHCID 59830414—

Reaction Steps

To a solution of 5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carboxylic acid (Preparation 5, 20.0 mg, 0.10 mmol) in DMF (5 mL) was added 3,4-dichlorobenzoic acid hydrazide (23 mg, 0.11 mmol), DIPEA (19.5 μL, 0.11 mmol) and HOBt (14.0 mg, 0.10 mmol). The resulting solution was stirred for 5 min prior to the addition of EDCI (23 mg, 1.20 mmol). The reaction mixture was stirred for 16 hr at rt then partitioned between water (10 mL) and dichloromethane (20 mL) on a hydrophobic frit. The aqueous phase was extracted with a further portion of dichloromethane (30 mL) and the combined organics were concentrated in vacuo. Trituration of the resulting residue with ethyl acetate/dichloromethane gave the title compound. δH (d6 DMSO): 12.25 (1H, s), 10.83 (2H, d), 8.17 (1H, s), 7.55-7.97 (3H, m), 7.38 (1H, s), 7.26 (1H, d); m/z (ES+)=383 [M+H]+; RT=3.37 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884112B2
Source datasetuspto-grants-2011_02
ORD IDord-64b229b7923f455bbdbe4bf51c715732
Source noteuspto-grants-2011_02