HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 12003970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | HCID 58815995 | HCID 58815995 | — |
| Product | HCID 12003970 | HCID 12003970 | 35.4% |
Reaction Steps
The title compound was made by a procedure identical to that of Example 60 using 1.0 g of 4-{3-[(R)-((2S,5R)-2,5-dimethyl-piperazin-1-yl)-(3-hydroxy-phenyl)-methyl]-benzoyl}-piperazine-1-carboxylic acid ethyl ester and 0.44 g of benzaldehyde (4.16 mmol, 2 equiv.) to give 0.42 g of the title compound as a light pink solid. 1H NMR (300 MHz, d6-DMSO): □ 1.00-1.01 (d, J=5.5 Hz, 6H); 1.14-1.19 (t, 3H), 1.56-2.00 (m, 2H); 2.48 (s, 4H); 2.56-2.65 (m, 4H); 3.39-3.51 (m, 5H); 3.72-3.76 (dd, 1H); 4.00-4.07 (q, 2H); 4.96 (s, 1H); 6.62-6.70 (m, 3H); 7.09-7.63 (m, 10H); 9.37 (s, 1H). Calculated for C34H42N4O4.0.44 CH2Cl2: C, 68.02; H, 7.11; N, 9.21. Found: C, 68.00; H, 7.20; N, 9.12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683168B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-fd3d48b7d99748cbacbb7318690396f0 |
| Source note | uspto-grants-2010_03 |