HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038058Generated: November 4, 2026
Potassium Hydroxide → HCID 59129248, compound
https://huagongshe.com/reaction/2038058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Water ethanol | HCID 19096565 | — |
| Reactant | HCID 59129283 | HCID 59129283 | — |
| Product | HCID 59129248 | HCID 59129248 | — |
Reaction Steps
A mixture of 1-(benzo[d][1,3]dioxol-5-yl)-N-(2-(4-cyano-2-methylbutan-2-yl)-1H-indol-5-yl)cyclopropanecarboxamide (0.060 g, 0.15 mmol) and KOH (0.081 g, 1.5 mmol) in 50% EtOH/water (2 mL) was heated in the microwave at 100° C. for 1 h. The solvent was evaporated under reduced pressure. The crude product was dissolved in DMSO (1 mL), filtered, and purified by reverse phase preparative HPLC to give 4-(5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indol-2-yl)-4-methylpentanoic acid. 1 H NMR (400 MHz, DMSO-d6) δ 11.98(s, 1H), 10.79(s, 1H), 8.44(s, 1H), 7.56(s, 1H), 7.15(d, J=8.6 Hz, 1H), 7.03-6.90(m, 4H), 6.05(s, 1H), 6.02(s, 2H), 1.97-1.87(m, 4H), 1.41-1.38(m, 2 H), 1.30(s, 6 H), 1.04-1.02(m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575209B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-6bfbc81c67c24dde98ef9aa7b92584b8 |
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| Source note | uspto-grants-2013_11 |
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