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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989872Generated: October 25, 2026

Diisopropylamine → (1,1'-Biphenyl)-2-carboxamide

https://huagongshe.com/reaction/1989872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantThionyl ChlorideHCID 24386—
Reactanto-Phenylbenzoic acidHCID 70357—
Reactant4-[1-(Phenylmethyl)-4-piperidinyl]-benzenamineHCID 22499396—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(1,1'-Biphenyl)-2-carboxamideHCID 83254253.5%

Reaction Steps

2-Biphenylcarboxylic acid (0.25 mol) was dissolved in DCM (500 ml) and DMF (0.5 ml). Thionyl chloride (0.51 mol) was added dropwise. The mixture was stirred and refluxed for 1 hour under nitrogen flow. The solvent was evaporated. DCM (500 ml) was added twice. The solvent was evaporated twice. The residue was dissolved in DCM (200 ml) and then added dropwise at 0° C. to a mixture of 4-[1-(phenylmethyl)-4-piperidinyl]-benzenamine (0.25 mol) and N-(1-methylethyl)-2-propanamine (0.75 mol) in DCM (800 ml). The mixture was brought to room temperature and then stirred at room temperature overnight under nitrogen flow. The mixture was washed three times with water (800 ml). The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 125 g of [1,1′-biphenyl]-2-carboxamide, N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-(intermediate 39).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642378B2
Source datasetuspto-grants-2010_01
ORD IDord-e652dd9fed5846eaa8cce00d70d967af
Source noteuspto-grants-2010_01