HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576284Generated: October 30, 2026
Potassium Carbonate → 3-(3-((6-Amino-1-naphthyl)oxy)propyl)-7-(2-methylphenyl)-1h-indole-2-carboxylic acid
https://huagongshe.com/reaction/576284
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylphenyl boronic acid | HCID 2733267 | — |
| Reactant | ethyl 3-(3-(6-aminonaphthalen-1-yloxy)propyl)-7-bromo-1H-indole-2-carboxylate | HCID 68938609 | — |
| Reactant | Methanol trifluoroacetic acid | HCID 86669916 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3-(3-((6-Amino-1-naphthyl)oxy)propyl)-7-(2-methylphenyl)-1h-indole-2-carboxylic acid | HCID 25144891 | — |
Reaction Steps
A mixture of EXAMPLE 563A (45 mg), o-tolylboronic acid (15.7 mg), K2CO3 (1 M, 0.17 ml) and bis(triphenylphosphine)palladium(II) dichloride (7.2 mg, 0.01 mmol) in a mixture of dimethoxyethane (2.2 ml), ethanol (0.6 ml) and water (0.9 ml) was heated at 160° C. in a microwave reactor (CEM Discover) for 10 minutes. The reaction mixture was acidified with a diluted trifluoroacetic acid methanol solution and concentrated. The residue was suspended in a mixture of DMSO and methanol (1:1) and filtered. The filtrate was purified by RP HPLC to provide the desired product. 1H NMR (400 MHz, DMSO-D6) δ 10.43 (s, 1 H), 8.08 (d, J=8.90 Hz, 1 H), 7.69 (d, J=6.75 Hz, 1 H), 7.31-7.34 (m, 2 H), 7.18-7.29 (m, 5 H), 7.02-7.11 (m, 5 H), 6.64 (d, J=7.67 Hz, 1 H), 4.15 (t, J=5.98 Hz, 2 H), 2.49-2.53 (m, 2 H), 2.17-2.25 (m, 2 H), 2.06 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035047B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-093604849b054c3b80282bc3d17fb99a |
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| Source note | uspto-grants-2015_05 |
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