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HRID 429523作成日:2026年10月25日

Hydroxypyridinone → Trocade

https://huagongshe.com/reaction/429523

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxypyridinoneHCID 69975—
反応物O-(Trimethylsilyl)hydroxylamineHCID 2734666—
反応物4-(2-Isocyanoethyl)morpholineHCID 2759434—
反応物1-[2(R)-[1(R)-carboxy-2-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]-3-cyclopentylpropionyl)piperdineHCID 11270129—
溶媒DichloromethaneHCID 6344—
生成物TrocadeHCID 982435083.3%

反応手順

0.78 g of 2-morpholino-ethyl isocyanide was added to a suspension of 2.11 g of 1-[2(R)-[1(R)-carboxy-2-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]-3-cyclopentylpropionyl]piperidine (IX) from Example 5 or 6 and 0.61 g of N-hydroxy-2-pyridone in 21 ml of methylene chloride at 22° and the mixture was stirred for 3 hrs. The solution was treated with 0.58 g of O-trimethylsilyl-hydroxylamine and stirred for 2 hrs. The reaction mixture was washed with saturated NaHCO3 solution and with water and evaporated. The residue was dissolved in 20 ml of tert-butyl methyl ether and 0.23 ml of water, stirred at 22° for 1½ hrs., the suspension was diluted with 10 ml of hexane, filtered and the residue was dried at 220/11 mbar, there being obtained 1.82 g (83%) of pure 1-[3-cyclopentyl-2(R)[1(R)-(hydroxycarbamoyl)-2-(3,4,4-trimethyl-2,5-dioxo-1-imidazolidinyl)ethyl]propionyl]piperidine (X), MS (EI): 436 (40%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06316633B1
出典データセットuspto-grants-2001_11
ORD IDord-37483557ea9e4fa39f2ade5c189efd7a
出典メモuspto-grants-2001_11