HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054865Generated: October 25, 2026
Methanesulfonamide → 6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-N-(methylsulfonyl)-1H-indole-3-carboxamide
https://huagongshe.com/reaction/1054865
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 3-Iodo-1,2-phenylene bis(2,2-dimethylpropanoate) | HCID 53431101 | — |
| Reactant | 6-Chloro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carbaldehyde | HCID 86698568 | — |
| Solvent | Isopropyl Acetate | HCID 7915 | — |
| Product | 6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-N-(methylsulfonyl)-1H-indole-3-carboxamide | HCID 71767986 | 13% |
Reaction Steps
To a mixture of 6-chloro-5-[4-(1-hydroxycyclobutyl)phenyl]-1H-indole-3-carbaldehyde (40 mg, 0.123 mmol), Bis(tert-butylcarbonyloxy)iodobenzene (104 mg, 0.256 mmol) in isopropyl acetate (2 mL) was added methanesulfonamide (12 mg, 0.126 mmol). After stirring 5 minutes, Bis[rhodium(α,α,α′,α′-tetramethyl-1,3-benzenedipropionic acid)] (5 mg, 0.007 mmol) was added and heated to 80° C. overnight. The mixture was concentrated to give a crude residue, which was purified by preparative HPLC to afford the title compound (6.6 mg, 13%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394285B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-d897d13c0b6b42089410cec31e5f5ad0 |
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| Source note | uspto-grants-2016_07 |
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