HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667188Generated: November 1, 2026
Benzhydrylpiperazine → HCID 67359031, compound
https://huagongshe.com/reaction/1667188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 67358235 | HCID 67358235 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67359031 | HCID 67359031 | — |
Reaction Steps
To a solution of 2-(4-(tert-butoxycarbonyl)-2-oxo-3-phenylpiperazin-1-yl)acetic acid (Example 101C, 0.334 g, 1 mmol) and 1-benzhydrylpiperazine (0.252 g, 1 mmol) in methylene chloride (10 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (0.38 g, 1 mmol) and diisopropylethylamine (0.8 mL). The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was then diluted with methylene chloride, and then washed sequentially with 1 N HCl, water, 1 N NaOH, and water. The organic layer was dried over magnesium sulfate and concentrated in vacuo to yield the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 7.44 (m, 6H), 7.30 (m, 7H), 7.19 (m, 2H), 5.74 (m, 1H), 4.51 (d, J=15.60 Hz, 1H), 4.23 (s, 1H), 4.12 (q, J=7.12 Hz, 1H), 3.96 (d, J=15.94 Hz, 1H), 3.59 (m, 3H), 2.38 (m, 5H), 1.44 (s, 9H); MS (ESI+) m/z 569 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044069B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-b9b4b5cee8fd46e2b48901517d5a512f |
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| Source note | uspto-grants-2011_10 |
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