HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486822Generated: October 26, 2026
N,N'-Dimethylethylenediamine → 1-(4-Chlorophenyl)-1H-pyrrolo[2,3-c]pyridine
https://huagongshe.com/reaction/1486822
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 6-Azaindole | HCID 9219 | — |
| Reactant | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Chlorophenyl)-1H-pyrrolo[2,3-c]pyridine | HCID 57402656 | 88.7% |
Reaction Steps
6-Azaindole (5.00 g, 42.3 mmol) was dissolved in DMF (150 mL) under nitrogen and 1-chloro-4-iodo-benzene (12.2 g, 50.8 mmol), N,N′-dimethylethylenediamine (911 uL, 8.46 mmol), K3PO4 (18.9 g, 88.9 mmol) and CuI (806 mg, 4.23 mmol) were added. The reaction mixture was heated at 150° C. for 18 h. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was suspended in 1M aq Na2CO3 (250 mL) and extracted into DCM (2×250 mL). The combined organic fractions were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography to give the title compound as a yellow solid (8.58 g, 88.6%). LCMS (ES+): 229.1 [MH]+. HPLC: Rt 4.48 min, 98.6% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428498B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ae685789ab95441f8748070d52557965 |
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| Source note | uspto-grants-2016_08 |
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