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

Triethylamine → Benzyl 2-{[(trifluoroacetyl)amino]methyl}morpholine-4-carboxylate

HRID 1371378
노트
인쇄 미리보기

반응식

HRID 1371378 반응식
[F:1][C:2]([F:14])([F:13])[C:3]([NH:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][NH:9][CH2:8]1)=[O:4].[CH2:15]([O:22][C:23](Cl)=[O:24])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(N(CC)CC)C>CO>[F:14][C:2]([F:13])([F:1])[C:3]([NH:5][CH2:6][CH:7]1[O:12][CH2:11][CH2:10][N:9]([C:23]([O:22][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:24])[CH2:8]1)=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 10387Benzyl chloroformateHCID 115502612,2,2-trifluoro-N-(morpholin-2-ylmethyl)acetamide

생성물 1

HCID 17984666Benzyl 2-{[(trifluoroacetyl)amino]methyl}morpholine-4-carboxylate

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
22 °C

실험 절차

To a stirred solution of Intermediate 1 (6.37 g) in methanol (250 ml) under nitrogen was added benzylchloroformate (4.7 ml) and triethylamine (6.3 ml). The mixture was stirred at 22° C. for 1 h before the volatiles were removed in vacuo. The residue was purified by Biotage flash chromatography on a 90 g silica cartridge eluting with 33% ethyl acetate in cyclohexane, to give the title compound as a white solid (4.4 g).

후처리

  1. customwere removed in vacuo
  2. customThe residue was purified by Biotage flash chromatography on a 90 g silica cartridge
  3. washeluting with 33% ethyl acetate in cyclohexane

출처 및 근거

ORD 기록
ord-568a120fde3c436e8fe42518c432a810
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157457B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트