HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018361Generated: November 1, 2026
HCID 18405518, compound → HCID 18405427, compound
https://huagongshe.com/reaction/1018361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18405518 | HCID 18405518 | — |
| Reactant | Methyl 3-aminocinnamate | HCID 54385173 | — |
| Product | HCID 18405427 | HCID 18405427 | — |
Reaction Steps
5-(2-Adamantan-1-yl-ethyl)-2-cyclohexyl-1H-imidazole-4-carboxylic acid (Example 252) was reacted with 3-(3-amino-phenyl)-acrylic acid methyl ester (prepared in two steps from 3-nitro-benzaldehyde) 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) 12.00 (1H, br s), 9.55 (1H, br s), 8.00 (1H, s), 7.86 (1H, m), 7.57 (1H, d), 7.36 (2H, m), 6.50 (1H, d), 2.89 (2H, m), 2.68 (1H, m), 1.94 (5H, br s), 1.80-1.51 (17H, m), 1.39-1.19 (5H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 60.52; H, 8.50; N, 7.59%. C38H56N4O8.3.0 mols H2O requires: C, 60.78; H, 8.32; N, 7.46%.
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-4254c27569894fd2ab90c21267e51c90 |
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| Source note | uspto-grants-2002_11 |
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