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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018367Generated: October 29, 2026

3-Nitrobenzoic acid → HCID 54968862, compound

https://huagongshe.com/reaction/1018367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrobenzoic acidHCID 8497—
ReactantHCID 52179919HCID 52179919—
ReactantHCID 86758603HCID 86758603—
ProductHCID 54968862HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479531B1
Source datasetuspto-grants-2002_11
ORD IDord-b01466857a6d42dba660c0b14ca10471
Source noteuspto-grants-2002_11