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

Diisopropylethylamine → Tert-butyl (+/-)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate

HRID 1424286
노트
인쇄 미리보기

반응식

HRID 1424286 반응식
[CH3:1][CH:2]([CH3:19])[CH2:3][C:4]([C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1)=O.[CH3:20][C:21]1[CH:22]=[N+:23]([O-])[C:24]2[C:29]([CH:30]=1)=[CH:28][CH:27]=[CH:26][CH:25]=2.C([N:35](C(C)C)CC)(C)C.F[P-](F)(F)(F)(F)F.Br[P+](N1CCCC1)(N1CCCC1)N1CCCC1>ClCCl.C(=O)(O)[O-].[Na+]>[CH3:1][CH:2]([CH3:19])[CH2:3][CH:4]([C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1)[NH:35][C:22]1[C:21]([CH3:20])=[CH:30][C:29]2[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=2)[N:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 70214663-Methylquinoline N-oxideHCID 71239698Tert-butyl 4-(3-methylbutanoyl)benzoate

생성물 1

HCID 71243814Tert-butyl (+/-)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate

시약·촉매·용매 2

HCID 6344
Dichloromethane
용매
HCID 516892Sodium Bicarbonate용매

실험 절차

To a solution of tert-butyl(+/−)-4-(3-methylbutanoyl)benzoate (527 mg, 2.00 mmol) and 3-methylquinoline N-oxide (318 mg, 2.00 mmol) in dichloromethane (8.0 mL) was added diisopropylethylamine (1.31 mL, 7.50 mmol) followed by bromotripyrrolidinophosphonium hexafluorophosphate (1.18 g, 2.50 mmol). The solution was stirred at room temperature for 18 hours then diluted with sat. aq sodium bicarbonate (20 mL). The mixture was extracted with ethyl acetate (3×20 mL). The combined organics were dried over anhydrous Na2SO4 and filtered, and the filtrate was concentrated. Purification by silica gel flash chromatography (ethyl acetate/heptane) gave tert-butyl(+/−)-4-(3-methyl-1-((3-methylquinolin-2-yl)amino)butyl)benzoate as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.94 (d, J=8.2 Hz, 2H), 7.63 (d, J=8.2 Hz, 1H), 7.59 (s, 1H), 7.54-7.48 (m, 3H), 7.47-7.41 (m, 1H), 7.19-7.13 (m, 1H), 5.56 (q, J=7.4 Hz, 1H), 4.73 (d, J=7.0 Hz, 1H), 2.28 (s, 3H), 1.94-1.83 (m, 1H), 1.81-1.70 (m, 1H), 1.70-1.60 (m, 1H), 1.57 (s, 9H), 1.04 (d, J=6.6 Hz, 3H), 0.97 (d, J=6.6 Hz, 3H).

후처리

  1. extractionThe mixture was extracted with ethyl acetate (3×20 mL)
  2. dry with materialThe combined organics were dried over anhydrous Na2SO4
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated
  5. customPurification by silica gel flash chromatography (ethyl acetate/heptane)

출처 및 근거

ORD 기록
ord-5e421d8a984e4b71876a24b41ffc34f5
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927577B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트