홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Hydroxide → N-cyclopropylmorpholine-2-carboxamide

HRID 1435501
노트
인쇄 미리보기

반응식

HRID 1435501 반응식
[OH-].[Na+].[CH:3]1([NH:6][C:7]([CH:9]2[O:14][CH2:13][CH2:12][N:11](C(OCC3C4C=CC=CC=4C4C3=CC=CC=4)=O)[CH2:10]2)=[O:8])[CH2:5][CH2:4]1>CO>[CH:3]1([NH:6][C:7]([CH:9]2[O:14][CH2:13][CH2:12][NH:11][CH2:10]2)=[O:8])[CH2:5][CH2:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 579373209H-fluoren-9-ylmethyl 2-[(cyclopropylamino)carbonyl]morpholine-4-carboxylate

생성물 1

HCID 57937375N-cyclopropylmorpholine-2-carboxamide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

NaOH (1 mL, 2 M, 2.0 mmol) was slowly added to a solution of 9H-fluoren-9-ylmethyl 2-[(cyclopropylamino)carbonyl]morpholine-4-carboxylate (1.0 g, 2.6 mmol) in MeOH (70 mL) at ambient temperature. The reaction mixture was stirred for 3 h and the solvent was concentrated. The product was recovered in water (50 mL) and the mixture was neutralized to pH 7 using HCl solution. The product was extracted with EtOAc and dried over anhydrous Na2SO4. The solvent was concentrated to provide the title compound that was used for the next step without further purification. Yield: 0.8 g.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. concentrationthe solvent was concentrated
  2. customThe product was recovered in water (50 mL)
  3. extractionThe product was extracted with EtOAc
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationThe solvent was concentrated

출처 및 근거

ORD 기록
ord-1b5ad828a35549a98d459a0e95eefa9e
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07615642B2

반응 노트

불러오는 중…