돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41103생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물DiisopropylethylamineHCID 81531—
반응물4-Fluoro-3-nitrotolueneHCID 136287—
반응물(R)-2-Aminomethyl-4-Boc-morpholineHCID 1515269—
촉매ZincHCID 23994—
용매MethanolHCID 887—
생성물(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylateHCID 6717027899.6%

반응 조건

온도140 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530467B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-48826e0ef53c44c2b9ad5f3907d5d719
출처 메모uspto-grants-2013_09