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

di-tert-butyl 4-(4-hydroxybenzyl)-L-glutamate → (4R)-4-(4-hydroxybenzyl)-L-glutamic acid

HRID 591333
노트
인쇄 미리보기

반응식

HRID 591333 반응식
[OH:1][C:2]1[CH:26]=[CH:25][C:5]([CH2:6][CH:7]([C:18]([O:20]C(C)(C)C)=[O:19])[CH2:8][C@@H:9]([C:11]([O:13]C(C)(C)C)=[O:12])[NH2:10])=[CH:4][CH:3]=1>FC(F)(F)C(O)=O.C1(C)C=CC=CC=1>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][C@@H:7]([C:18]([OH:20])=[O:19])[CH2:8][C@@H:9]([C:11]([OH:13])=[O:12])[NH2:10])=[CH:25][CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 70977414di-tert-butyl 4-(4-hydroxybenzyl)-L-glutamate

생성물 1

HCID 70977181(4R)-4-(4-hydroxybenzyl)-L-glutamic acid

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6422Trifluoroacetic acid용매

실험 절차

Di-tert-butyl 4-(4-hydroxybenzyl)-L-glutamate (27 mg, 58 μmol) was dissolved in trifluoroacetic acid (1 ml) and stirred at room temperature for 2 h. The mixture was then taken up in toluene and concentrated under reduced pressure. The residue was purified by preparative HPLC (RP-18; solvents: acetonitrile (+0.1% trifluoroacetic acid), water (+0.1% trifluoroacetic acid); gradient: 30%->40% acetonitrile (20 min)).

후처리

  1. concentrationconcentrated under reduced pressure
  2. customThe residue was purified by preparative HPLC (RP-18; solvents: acetonitrile (+0.1% trifluoroacetic acid), water (+0.1% trifluoroacetic acid); gradient: 30%->40% acetonitrile (20 min))

출처 및 근거

ORD 기록
ord-fd7030a20eb14ff5b7b5b239a4e945e2
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238631B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트