HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018360Generated: November 1, 2026
HCID 18405518, compound → HCID 18405676, compound
https://huagongshe.com/reaction/1018360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18405518 | HCID 18405518 | — |
| Reactant | HCID 53948864 | HCID 53948864 | — |
| Product | HCID 18405676 | HCID 18405676 | — |
Reaction Steps
5-(2-Adamantan-1-yl-ethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid (Example 252) was reacted with 1-(3-amino-phenyl)-1-cyclopentanecarboxylic acid ethyl ester (prepared from 1-(4-chloro-phenyl)-1-cyclopentanecarboxylic acid using Mutti's procedure (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) 12.00 (1H, br s), 9.29 (1H, br s), 7.63 (2H, m), 7.16 (1H, m), 7.02 (1H, d), 2.85 (2H, m), 2.49 (3H, m), 1.98-1.34 (33H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 62.88; H, 8.79; N, 7.07%. C41H62N4O8.2.5 mols H2O requires: C, 62.81; H, 8.61; N, 7.15%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479531B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-74138cf70a1046179149781f6aca1317 |
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| Source note | uspto-grants-2002_11 |
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