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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553782Generated: November 1, 2026

N-methyl-2-pyrrolidone → 4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid (1-methyl-2-morpholin-4-yl-ethyl)-amide

https://huagongshe.com/reaction/553782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(S)-4-(2-Amino-propan-1-yl)-morpholineHCID 7004115—
Reactant4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acidHCID 57851511—
SolventDichloromethaneHCID 6344—
Product4'-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid (1-methyl-2-morpholin-4-yl-ethyl)-amideHCID 2488948181%

Reaction Conditions

Temperature0 °C

Reaction Steps

EDCI (54.0 mg, 0.282 mmol) was added in one portion at 0° C. to a solution of 4′-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid (60.0 mg, 0.214 mmol), HOBt (40.0 mg, 0.296 mmol) and NMP (101.5 mg, 1.000 mmol) in CH2Cl2 (3 mL). After the reaction stirred at 0° C. for 1 hour, (S)-1-Methyl-2-morpholin-4-yl-ethylamine (50.0 mg, 0.230 mmol) was added. The reaction mixture was allowed to warm to room temperature and was stirred overnight. Solvent was removed under reduced pressure and the residue was purified by column chromatography (EtOAc) to afford 4′-Methyl-5-tetrazol-1-yl-biphenyl-3-carboxylic acid (1-methyl-2-morpholin-4-yl-ethyl)-amide as a white solid (70 mg, 81%). MS (M+H)=407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048905B2
Source datasetuspto-grants-2011_11
ORD IDord-abd3f3c56d944fb0b95d813f27452cf0
Source noteuspto-grants-2011_11