HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898290Generated: October 31, 2026
HCID 57942589, compound → HCID 58268249, compound
https://huagongshe.com/reaction/1898290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57942589 | HCID 57942589 | — |
| Reactant | HCID 58268032 | HCID 58268032 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58268249 | HCID 58268249 | 145% |
Reaction Steps
To a solution of N-(2-Bromo-5-chloro-6-methyl-pyridin-3-yl)-4-chloro-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide (152.7 mg, 0.3 mmol) in 2 ml of THF under nitrogen atmosphere at 0° C. was added via syringe 2.0M isopropyl magnesium chloride (0.36 ml, 0.72 mmol). The reaction mixture was stirred for about 45 minutes and 1-(tert-Butyl-dimethyl-silanyl)-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde (54 mg, 0.21 mmol) was added and the resultant mixture was stirred for 30 minutes at 0° C. and then 2 hours at room temperature. The mixture was quenched with saturated ammonium chloride and extracted with ethyl acetate. The organic layer was separated and washed with water twice and dried. Concentration of this mixture afforded the crude product (210 mg) which was used in the next step without any further purification. MS (ES) (M++H) expect 689. found 688.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519135B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a2f24d868d604e9d80c67f3fb0d1bfa6 |
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| Source note | uspto-grants-2013_08 |
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