HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18405518, compound → HCID 57231403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18405518 | HCID 18405518 | — |
| Reactant | HCID 57089458 | HCID 57089458 | — |
| Product | HCID 57231403 | HCID 57231403 | — |
Reaction Steps
3-(5-Amino-2-chloro-phenyl)-acrylic acid methyl ester (prepared in two steps from 2-chloro-5-nitro-benzaldehyde) was reacted with 5-(2-adamantan-1-yl-ethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid (Example 252) according to the procedure of Example 20, step d. The methyl ester was hydrolysed using the same procedure as in Example 36, step d to afford the title compound. 1H NMR (300 MHz, d6-DMSO) 10.80 (1H, br s), 8.25 (1H, d), 7.96 (1H, d), 7.87 (1H, d), 7.55 (1H, d), 6.44 (1H, d), 2.94 (3H, m), 1.98-1.33 (27H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 55.45; H, 7.91; N, 6.97%. C38H55ClN4O8.5.0 mols H2O requires: C, 55.57; H, 7.98; N, 6.82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479531B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-d02df034bb9b4b4ebcc1a842e9238416 |
| Source note | uspto-grants-2002_11 |