HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717079Generated: October 30, 2026
HCID 14901692, compound → HCID 71735151, compound
https://huagongshe.com/reaction/717079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 14901692 | HCID 14901692 | — |
| Reactant | HCID 16895372 | HCID 16895372 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71735151 | HCID 71735151 | 13.7% |
Reaction Steps
3-Chloro-N,N-diethyl-2-methyl-benzamide (150 mg, 0.66 mmol) was dissolved in anhydrous THF (2 mL) under N2 and cooled to −78° C. n-BuLi (2.5M in n-hexanes, 558 μL, 1.39 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for 30 minutes. 4-Cyano-N-(1-methyl-piperidin-4-ylmethyl)-benzamide (180 mg, 0.66 mmol) in anhydrous THF (2 mL) was added dropwise to the reaction mixture and stirred at −78° C. continued for 1 h. The reaction mixture was poured into ice/water, allowed to warm to RT and extracted with CH2Cl2 (×3) and the organic phase dried (MgSO4). The solution was filtered and concentrated in vacuo. The crude material was purified by reverse phase preparative HPLC-MS to afford 4-(5-chloro-1-oxo-1,2-dihydro-isoquinolin-3-yl)-N-(1-methyl-piperidin-4-ylmethyl)-benzamide as a white solid (37 mg, 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193689B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-cf924d25813e4e2da0a4834f9aca1324 |
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| Source note | uspto-grants-2015_11 |
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