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HRID 712451作成日:2026年10月24日

Water → Tetrahydro-6-(phenylmethyl)-1H-pyrrolo(3,4-b)pyridine-5,7(2H,6H)-dione

https://huagongshe.com/ja/reaction/712451

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物6-Benzyl-5,7-dihydro-5,7-dioxopyrrolo[3,4-b]pyridineHCID 289502—
触媒PalladiumHCID 23938—
溶媒2-MethoxyethanolHCID 8019—
生成物Tetrahydro-6-(phenylmethyl)-1H-pyrrolo(3,4-b)pyridine-5,7(2H,6H)-dioneHCID 989960460%

反応条件

温度90 °C

反応手順

To a solution of 6-benzyl-5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione (5.00 g) in glycol monomethyl ether was added a catalytic amount of 10% Pd/C. The reaction mixture was heated to 90° C. and stirred for 6 h under H2, then cooled to rt. The resulted mixture was poured into 100 mL of water and extracted with CH2Cl2 (50 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 1:2 (v/v) PE/EA) to give the title compound as colorless oil (3.00 g, 60.00%), HPLC: 95.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 245.1 (M+1); 1H NMR (400 MHz, CDCl3) δ: 1.47-1.53 (m, 4H), 2.12 (s, 1H), 2.63-2.69 (m, 1H), 2.76-2.88 (m, 2H), 3.83 (d, J=8.2, 2H), 4.64 (s, 1H), 7.25-7.36 (m, 5H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181277B2
出典データセットuspto-grants-2015_11
ORD IDord-371f326cff5f42b990e6ff8984c86e89
出典メモuspto-grants-2015_11