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HRID 41103作成日:2026年10月24日

Acetic Acid → (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/ja/reaction/41103

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物DiisopropylethylamineHCID 81531—
反応物4-Fluoro-3-nitrotolueneHCID 136287—
反応物(R)-2-Aminomethyl-4-Boc-morpholineHCID 1515269—
触媒ZincHCID 23994—
溶媒MethanolHCID 887—
生成物(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylateHCID 6717027899.6%

反応条件

温度140 °C

反応手順

A mixture of (R)-tert-butyl 2-(aminomethyl)morpholine-4-carboxylate (0.715 g, 3.31 mmol), DIPEA (0.577 mL, 3.31 mmol), and 1-fluoro-4-methyl-2-nitrobenzene (0.513 g, 3.31 mmol) in MeOH (14 mL) was heated at 140° C. in A microwave reactor for 30 min and then cooled to room temperature. Acetic acid (1.9 mL, 33.1 mmol) was added, followed by zinc (2.162 g, 33.1 mmol). The resulting mixture was stirred at room temperature for 90 min to afford the (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate product (1.06 g), which was used without further purification in the next step. The product was analyzed on analytical HPLC MS using the high pH gradient method (mobile phase: 5-95% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v; B: CH3CN; 2.25 min run; X-Bridge C18; column size: 2.1×30 mm; and particle size: 5 μm). MS m/z 322.4 [M+H]+ (ESI), Rt 1.80 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530467B2
出典データセットuspto-grants-2013_09
ORD IDord-48826e0ef53c44c2b9ad5f3907d5d719
出典メモuspto-grants-2013_09