HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18405518, compound → HCID 18405440, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18405518 | HCID 18405518 | — |
| Reactant | HCID 54475761 | HCID 54475761 | — |
| Product | HCID 18405440 | HCID 18405440 | — |
Reaction Steps
5-(2-Adamantan-1-yl-ethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid (Example 252) was reacted with (±)-2-(3-amino-phenyl)-propionic acid ethyl ester (S. Mutti et al. Synth. Comm. 1997, 27, 425) according to the procedure of Example 20, step d. The ethyl ester was hydrolysed using the same procedure as in Example 247, step b to afford the title compound. 1H NMR (300 MHz, d6-DMSO) 12.20 (2H, br s), 9.44 (1H, s), 7.64 (2H, m), 7.23 (1H, m), 6.96 (1H, d), 3.61 (1H, m), 2.86 (2H, m), 2.60 (1H, m), 1.98-1.19 (30H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 62.88; H, 8.66; N, 7.68%. C38H58N4O8.1.5 mols H2O requires: C, 62.87; H, 8.47; N, 7.72%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479531B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-9d9b38c590ad46a79b2c8e638d3f05b4 |
| Source note | uspto-grants-2002_11 |