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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49555Generated: October 26, 2026

Benzoic acid, 2-amino-5-iodo- → benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide

https://huagongshe.com/reaction/49555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 2-amino-5-iodo-HCID 72911—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromideHCID 68830145—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productbenzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamideHCID 6883052412.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

The above material, (61b), N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide (59 mg) was dissolved in DMF (1 mL). After cooling to 0° C., diisopropylethylamine (0.1 mL) and 2-amino-5-iodobenzoic acid (43 mg) were added. BOP Reagent (72 mg) was added, and the mixture was stirred overnight. EtOAc was added along with NaHCO3 solution. The EtOAc was dried (MgSO4), filtered, and concentrated. Reverse phase HPLC purification (gradient elution, water/acetonitrile/TFA) of the resulting residue provided the title benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide (6 mg). MS found: (M+Na)+=622.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706712B2
Source datasetuspto-grants-2004_03
ORD IDord-2293be807c014f698d93db400192cb82
Source noteuspto-grants-2004_03