戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1989872作成日:2026年10月27日

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

https://huagongshe.com/reaction/1989872

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Thionyl ChlorideHCID 24386—
反応物o-Phenylbenzoic acidHCID 70357—
反応物4-[1-(Phenylmethyl)-4-piperidinyl]-benzenamineHCID 22499396—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物(1,1'-Biphenyl)-2-carboxamideHCID 83254253.5%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07642378B2
出典データセットuspto-grants-2010_01
ORD IDord-e652dd9fed5846eaa8cce00d70d967af
出典メモuspto-grants-2010_01