HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677436Generated: October 31, 2026
7-iodo-5-triisopropylsilanyl-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine → 2-methoxy-2-methyl-1-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-propan-1-one
https://huagongshe.com/reaction/1677436
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-iodo-5-triisopropylsilanyl-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine | HCID 59540525 | — |
| Reactant | N,2-Dimethoxy-N,2-dimethylpropanamide | HCID 86646687 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-methoxy-2-methyl-1-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-propan-1-one | HCID 59540952 | 9% |
Reaction Steps
A solution of 7-iodo-5-triisopropylsilanyl-2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazine (233 mg, 0.410 mmol) in anhydrous tetrahydrofuran (3 ml) was cooled to −78° C. and treated with nBuLi (2.29M in hexanes, 0.25 ml, 0.57 mmol) dropwise. The solution was stirred for 30 seconds and then 2,N-dimethoxy-2,N-dimethyl-propionamide (198 mg, 1.23 mmol), dissolved in THF (5 ml), was added dropwise. The reaction mixture was stirred at −78° C. for 30 minutes and then at room temperature 30 minutes. The reaction mixture was quenched with saturated aqueous NaHSO4 and then partitioned between EtOAc/water. The organic layers were collected, dried over MgSO4, filtered, and concentrated giving a brown oil. The oil was purified by silica gel chromatography using 10-100% EtOAc in hexanes as eluant providing 14 mg (9%) of 2-methoxy-2-methyl-1-[2-(3,4,5-trimethoxy-phenyl)-5H-pyrrolo[2,3-b]pyrazin-7-yl]-propan-1-one as a yellow solid. MP 237.8-239.1° C., M+H=386.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008298B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-0ed29aca71fe433c970184a7ab7de99a |
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| Source note | uspto-grants-2011_08 |
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