HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646105Generated: October 30, 2026
N,N'-Dimethylethylenediamine → 1-(4-Isopropoxyphenyl)-5-(6-isopropoxypyrid-3-yl)indole-2-carb-oxylic acid ethyl ester
https://huagongshe.com/reaction/646105
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Bromo-4-(propan-2-yloxy)benzene | HCID 228088 | — |
| Reactant | 5-(6-Isopropoxypyrid-3-yl)indole-2-carboxylic acid ethyl ester | HCID 68699460 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Isopropoxyphenyl)-5-(6-isopropoxypyrid-3-yl)indole-2-carb-oxylic acid ethyl ester | HCID 68698234 | 70% |
Reaction Steps
A mixture of CuI (7.14 mg, 51 mmol), N,N′-dimethyl-1,2-diaminoethane (16.7 μL, 0.153 mmol) and toluene (0.5 mL) was added to a mixture of 5-(6-isopropoxypyrid-3-yl)indole-2-carboxylic acid ethyl ester (165 mg, 0.510 mmol; see step (a)), 1-bromo-4-isopropoxybenzene (219 mg, 1.02 mmol), K3PO4 (108 mg, 0.510 mmol) and toluene (2 mL) under argon. The mixtures was heated at 110° C. for 5 h and at 140° C. for 16 h, then allowed to cool to room temperature and filtered through Celite®. The filter cake was washed with EtOAc and the combined filtrates were concentrated and purified by chromatography to give the sub-title compound (163 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07705023B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-74250d38cf034607bba27150bbd648bc |
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| Source note | uspto-grants-2010_04 |
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