HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 5-amino-2-fluorobenzoate → HCID 18405481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 5-amino-2-fluorobenzoate | HCID 15621043 | — |
| Reactant | HCID 18405518 | HCID 18405518 | — |
| Product | HCID 18405481 | HCID 18405481 | — |
Reaction Steps
5-(2-Adamantan-1-yl-ethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid (Example 252) was reacted with 5-amino-2-fluoro-benzoic acid methyl ester 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) 10.79 (1H, br s), 8.32 (1H, dd), 7.97 (1H, m), 7.32 (1H, m), 2.91 (3H, m), 1.98-1.34 (27H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 56.04; H, 8.48; N, 7.28%. C36H53FN4O8.4.5 mols H2O requires: C, 56.16; H, 8.12; N, 7.28%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479531B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-33489d6c32fb43878351a7862a02bfae |
| Source note | uspto-grants-2002_11 |