HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16763Generated: October 30, 2026
Sodium bis(trimethylsilyl)amide → HCID 178489761, compound
https://huagongshe.com/reaction/16763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | Tert-butyl 5-amino-3-[2-(3,5-dimethoxyphenyl)ethyl]pyrazole-1-carboxylate | HCID 57440371 | — |
| Reactant | Methyl 4-(3,5-dimethylpiperazin-1-yl)benzoate | HCID 57440402 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178489761 | HCID 178489761 | 10.5% |
Reaction Steps
N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]-4-(3,5-dimethylpiperazin-1-yl)benzamide was prepared as for Example 94, but starting from methyl 4-(3,5-dimethylpiperazin-1-yl)benzoate (221 mg, 0.84 mmol ), tert-butyl 5-amino-3-[2-(3,5-dimethoxyphenyl)ethyl]-1H-pyrazole-1-carboxylate (244 mg, 0.7 mmol) and 1M NaHMDS (1.13 ml, 1.13 mmol) in THF (5 ml). The crude product was purified by reverse phase prep. HPLC (basic) using a 34-54% gradient of acetonitrile in water containing 1% 0.880 ammonia. The clean fractions were taken and evaporated to afford the title compound as a white solid (34 mg, 10%); 1H NMR (399.9 MHz, DMSO-d6) δ 1.04 (6H, d), 2.22 (2H, t), 2.53 (2H, d), 2.82 (2H, t), 2.87 (4H, s), 3.71 (1H, s), 3.73 (7H, s), 6.33 (1H, t), 6.42 (2H, d), 6.44 (1H, s), 6.94 (2H, d), 7.89 (2H, d), 10.27 (1H, s), 12.07 (1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737149B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-07a4293b9e11412fa0647f295efb95be |
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| Source note | uspto-grants-2010_06 |
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