HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054477Generated: October 30, 2026
HCID 22663271, compound → HCID 22663214, compound
https://huagongshe.com/reaction/2054477
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22663271 | HCID 22663271 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22663214 | HCID 22663214 | — |
Reaction Steps
A stirred solution of N-(3,5-dichloro-pyridin-4-yl)-3-formyl-1-(toluene-4-sulphonyl)-1H-indole-6-carboxamide (0.1 g, Example 17) in tetrahydofuran (3 ml), at 0° C., was treated with a solution of methylmagnesium bromide in diethyl ether (0.11 ml, 3M). The mixture was allowed to warm to room temperature then stirred for 2 hours. The reaction mixture was quenched with water (15 ml) and then extracted with ethyl acetate (15 ml). The organic extract was dried over sodium sulphate then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (2:1, v/v) to yield the title compound (68 mg) as a white solid, m.p. 206-211° C. [Elemental analysis:—C, 55.07; H, 4.00; N, 7.92%. Calculated for C23H19Cl2N3O4S:—C, 54.77; H, 3.80; N, 8.33%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329675B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-385552b5f8bf4a16a49fab041c947b7d |
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| Source note | uspto-grants-2008_02 |
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