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HRID 1005329作成日:2026年10月26日

Phenyl isocyanate → N-phenylquinuclidin-3-yloxycarboxamide

https://huagongshe.com/reaction/1005329

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl isocyanateHCID 7672—
反応物(+-)-3-QuinuclidinolHCID 15381—
生成物N-phenylquinuclidin-3-yloxycarboxamideHCID 394513186%

反応手順

1-Azabicyclo[2.2.2]octan-3-ol and phenyl isocyanate were used. The residual solid resulting from the above described procedure was purified via column chromatography eluting with a 1:10 ratio of methanol:chloroform to afford the title compound (86%) as a white solid: NMR (CDCl3) δ7.60-7.0 (m, 5H, Ph), 4.81 (m, 1H, CH--OCO), 3.27 (m, 1H, one of NCH2C--O), 2.9 (m, 5H, N(CH2)2 and one of NCH2C--O), 2.1 (m, 1H, methine at C4), 2.05-1.30 (m, 4H, CH2 at C5 and C8); FAB LRMS m /z (relative intensity, %) 247 ([MH+ ], 100).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06054464
出典データセットuspto-grants-2000_04
ORD IDord-60ee0a551127411a82db7f4a367de33e
出典メモuspto-grants-2000_04