HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504780Generated: October 26, 2026
Pyridine-2-sulfonyl Chloride → ethyl 5-(3-methoxypropoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylate
https://huagongshe.com/reaction/504780
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine-2-sulfonyl Chloride | HCID 3787675 | — |
| Reactant | ethyl 7-amino-5-(3-methoxypropoxy)-1H-indole-2-carboxylate | HCID 57476210 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | ethyl 5-(3-methoxypropoxy)-7-[(pyridin-2-ylsulfonyl)amino]-1H-indole-2-carboxylate | HCID 57476212 | 90.4% |
Reaction Steps
To a mixture of ethyl 7-amino-5-(3-methoxypropoxy)-1H-indole-2-carboxylate (3.00 g) and pyridine (50 mL) was added pyridine-2-sulfonyl chloride (2.0 g) at 0° C., and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated, 1N hydrochloric acid and ethyl acetate were added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed successively with water and saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography, and eluted with hexane-ethyl acetate (2:1-1:1, volume ratio) to give the title compound (4.02 g, yield 90%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane to give colorless prism crystals. melting point 126-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777047B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-d13c534556a74c81974a56930e9ccc10 |
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| Source note | uspto-grants-2010_08 |
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