HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379832Generated: October 30, 2026
HCID 18368038, compound → HCID 18368014, compound
https://huagongshe.com/reaction/379832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18368038 | HCID 18368038 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | HCID 18368014 | HCID 18368014 | — |
Reaction Steps
A mixture of 3-acetylamino-6-chloro-2-(3-carboxybenzoyl)indole (Example 132, 0.9 g, 2.5 mmol) and 10% HCl—MeOH (30 ml) was heated at 60° C. for 8 h. The mixture was cooled and concentrated, and the residue partitioned between water (100 ml) and ethyl acetate (100 ml). The organic layer was separated and washed with brine (50 ml), and dried (MgSO4) and solvent removed by evaporation. The residual solid was purified by flash column chromatography eluting with hexane/ethyl acetate (2/1) to afford 0.5 g of a title compound as a yellow solid. m.p.: 187-189° C. (ethyl acetate/hexane) 1H-NMR (DMSO-d6) δ: 9.14 (1H, br s), 8.47 (1H, dd, J=1.8, 1.1 Hz), 8.20 (1H, ddd, J=7.7, 1.8, 1.1 Hz), 8.03 (1H, ddd, J=7.7, 1.8, 1.1 Hz), 7.69-7.58 (2H, m), 7.28 (1H, d, J=1.8 Hz), 6.97 (1H, dd, J=1.4, 8.4 Hz), 6.04 (2H, br s), 3.95 (3H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06300363B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-d4adb608a3144c429e699a14661d7b23 |
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| Source note | uspto-grants-2001_10 |
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