HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096659Generated: November 3, 2026
HCID 68097900, compound → HCID 66786540, compound
https://huagongshe.com/reaction/1096659
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68097900 | HCID 68097900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66786540 | HCID 66786540 | 37.9% |
Reaction Steps
tert-Butyl (R)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxo-1-(4-(3-oxo-4-phenylpiperazin-1-yl)phenyl)butan-2-ylcarbamate (123A) (0.29 mmole, 206 mg) in DCM (10 mL) was added TEA (2 mL). The reaction solution was stirred at rt for 1 hr and then concentrated in vacuo. The residue was purified by preparative LC/MS (45-55% CH3CN in H2O) to afford 4-(4-((R)-2-Amino-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutyl)phenyl)-1-phenylpiperazin-2-one (233) (0.11 mmole, 14 mg, two-step yield: 7.9%). ESI-MS: m/z 609.5 (M+H)+. 1H NMR (400 MHz, MeOD) δ ppm 1.54-1.83 (m, 1H) 1.87-2.15 (m, 3H) 2.18-2.38 (m, 3H) 2.61-2.80 (m, 1H) 2.80-2.91 (m, 1H) 2.93-3.05 (m, 2H) 3.10-3.24 (m, 2H) 3.26 (s, 3H) 3.33-3.59 (m, 4H) 3.68 (t, J=5.43 Hz, 1H) 3.74-4.09 (m, 4H) 4.49-4.78 (m, 3H) 4.84 (br. s., 1H) 6.94-7.08 (m, 1H) 7.15-7.30 (m, 2H) 7.30-7.39 (m, 2H) 7.40-7.55 (m, 3H) 7.55-7.70 (m, 3H) 7.76-7.86 (m, 1H) 7.88-7.99 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138168B1 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-2226b14e1a33487f93e2c92db65e955d |
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| Source note | uspto-grants-2012_03 |
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