HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206108Generated: November 3, 2026
N-bromobutanimide → HCID 131735833, compound
https://huagongshe.com/reaction/2206108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 131735831 | HCID 131735831 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131735833 | HCID 131735833 | 77% |
Reaction Steps
To a solution of 7-methoxy-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-c]pyridine-4-carbonitrile (1.34 g) in ethyl acetate (20.15 mL) was added NBS (1.97 g) at room temperature, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.30 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371320B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-3d4826117f774ea5aa9535597dddc705 |
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| Source note | uspto-grants-2016_06 |
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