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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,4-Dichlorobenzhydrazide | HCID 311996 | — |
| Reactant | 5-chloro-1H-pyrrolo(3,2-b)pyridine-2-carboxylic acid | HCID 11665585 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,4-Dichlorobenzoic acid N'-(5-chloro-1H-pyrrolo[3,2-b]pyridine-2-carbonyl)hydrazide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884112B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-64b229b7923f455bbdbe4bf51c715732 |
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| Source note | uspto-grants-2011_02 |
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