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

Diisobutylaluminumhydride → 4-Isopropyl-1-piperidin-4-yl-1,3-dihydro-2H-imidazol-2-one

HRID 1867595
노트
인쇄 미리보기

반응식

HRID 1867595 반응식
[H-].C([Al+]CC(C)C)C(C)C.C(OC([N:18]1[CH2:23][CH2:22][CH:21]([NH:24][C:25]([NH:27][C@H:28]([C:32](OC)=O)[CH:29]([CH3:31])[CH3:30])=[O:26])[CH2:20][CH2:19]1)=O)(C)(C)C>C1(C)C=CC=CC=1.ClCCl>[CH:29]([C:28]1[NH:27][C:25](=[O:26])[N:24]([CH:21]2[CH2:20][CH2:19][NH:18][CH2:23][CH2:22]2)[CH:32]=1)([CH3:30])[CH3:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21225700DiisobutylaluminumhydrideHCID 68565788Methyl N-{[(1-tert-butoxycarbonylpiperidin-4-yl)amino]carbonyl}valinate

생성물 1

HCID 579795744-Isopropyl-1-piperidin-4-yl-1,3-dihydro-2H-imidazol-2-one

시약·촉매·용매 2

HCID 1140Toluene용매HCID 6344Dichloromethane용매

실험 절차

Diisobutylaluminum hydride (1M, 0.520 mL, 0.520 mmol) was added to a solution of methyl N-{[(1-tert-butoxycarbonylpiperidin-4-yl)amino]carbonyl}valinate (155 mg, 0.434 mmol) in toluene (3 mL) and dichloromethane (3 mL) at −78° C. and stirred for 30 min and then warmed to ambient temperature. After 1 h, the reaction was quenched with 1 N saturated potassium sodium tartrate solution (3 mL) and extracted with dichloromethane (2×). The combined organic extracts were dried over sodium sulfate, filtered, concentrated. The crude material was dissolved in dichloromethane (5 mL) and treated with trifluoroacetic acid (5 mL). After 30 min, the reaction was concentrated to give the title compound. MS 210.1 (M+1)

후처리

  1. waitAfter 1 h
  2. customthe reaction was quenched with 1 N saturated potassium sodium tartrate solution (3 mL)
  3. extractionextracted with dichloromethane (2×)
  4. dry with materialThe combined organic extracts were dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe crude material was dissolved in dichloromethane (5 mL)
  8. additiontreated with trifluoroacetic acid (5 mL)
  9. waitAfter 30 min
  10. concentrationthe reaction was concentrated

출처 및 근거

ORD 기록
ord-19582129592d44ab8171185a5540c85a
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07632832B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트