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HRID 2046073作成日:2026年10月25日

Glycine, N-methyl-, hydrochloride (1:1) → N-(4-(3-((4-Fluorophenyl)(isopropyl)amino)propyl)benzyl)-2,2-dimethyl-1,3-dioxan-5-amine

https://huagongshe.com/reaction/2046073

反応式

関与物質

役割名称HCID仕込み量
反応物Glycine, N-methyl-, hydrochloride (1:1)HCID 69483—
反応物2,2-Dimethyl-1,3-dioxan-5-amineHCID 11768608—
反応物4-(3-((4-Fluorophenyl)(isopropyl)amino)propyl)benzaldehydeHCID 86660609—
反応物4-(5-(((4-Fluorophenyl)(isopropyl)amino)methyl)thiophen-2-yl)benzaldehydeHCID 86660611—
生成物N-(4-(3-((4-Fluorophenyl)(isopropyl)amino)propyl)benzyl)-2,2-dimethyl-1,3-dioxan-5-amineHCID 6661491848%

反応手順

When the product of Step C and 2,2-dimethyl-1,3-dioxan-5-amine were substituted for 4-(5-(((4-fluorophenyl)(isopropyl)amino)methyl)-thiophen-2-yl)benzaldehyde and sarcosine hydrochloride in Example 22, Step C, the similar process afforded the title compound in 48% yield, as creamy paste. 1H-NMR (CDCl3) 7.24 (d, 2H, J=7.92 Hz), 7.11 (d, 2H, J=7.92 Hz), 6.87 (t, 2H, J=8.9 Hz), 6.69-6.62 (m, 2H), 3.95 (dd, 2H, J=11.7, 3.6 Hz), 3.83-3.69 (m, 4H), 3.06 (t, 2H, J=7.54 Hz), 2.66-2.58 (m, 3H), 1.83-1.76 (m, 3H), 1.41 (s, 3H), 1.4 (s, 3H), 1.08 (d, 2H, J=6.59 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08592399B2
出典データセットuspto-grants-2013_11
ORD IDord-f0c603b434b54c3e806beb6f2ef21fef
出典メモuspto-grants-2013_11