HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018367Generated: October 29, 2026
3-Nitrobenzoic acid → HCID 54968862, compound
https://huagongshe.com/reaction/1018367
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Nitrobenzoic acid | HCID 8497 | — |
| Reactant | HCID 52179919 | HCID 52179919 | — |
| Reactant | HCID 86758603 | HCID 86758603 | — |
| Product | HCID 54968862 | HCID 54968862 | — |
Reaction Steps
3-Nitro-benzoic acid was reacted with sarcosine ethyl hydrochloride and the resulting [(3-nitro-benzoyl)-methyl-amino]-acetic acid ethyl ester was hydrogenated to afford [(3-amino-benzoyl)-methyl-amino]-acetic acid ethyl ester. This 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 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) 10.79 (1H, br s), 7.83 (2H, m), 7.44 (1H, m), 7.14 and 7.01 (1H, 2×m), 4.15 and 3.97 (2H, 2×s), 2.94 (6H, m), 2.03-1.25 (27H, m). The acid was converted to the N-methyl-D-glucamine salt and lyophilised from water/dioxan. Found: C, 60.14; H, 8.24; N, 8.97%. C39H59N5O9.2.0 mols H2O requires: C, 60.21; H, 8.16, N 9.00%.
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-b01466857a6d42dba660c0b14ca10471 |
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| Source note | uspto-grants-2002_11 |
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