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

Triphenyl phosphite → 10-Oxo-1,3,4,9,10,10a-hexahydro-2,4-a,5,9-tetraaza-phenanthrene-2,7-dicarboxylic acid 2-tert-butyl ester 7-methyl ester

HRID 69673
노트
인쇄 미리보기

반응식

HRID 69673 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][NH:11][CH:10]([C:14]([OH:16])=O)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl[C:18]1[C:27]([N+:28]([O-])=O)=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][N:19]=1.C([O-])([O-])=O.[K+].[K+].P(OC1C=CC=CC=1)(OC1C=CC=CC=1)OC1C=CC=CC=1.[H][H]>C1COCC1.C(Cl)Cl.N.O[V](=O)=O.[Pt]>[CH3:25][O:24][C:22]([C:21]1[CH:26]=[C:27]2[C:18]([N:11]3[CH:10]([C:14](=[O:16])[NH:28]2)[CH2:9][N:8]([C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:13][CH2:12]3)=[N:19][CH:20]=1)=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 5

HCID 7540Triphenyl phosphiteHCID 11430Potassium CarbonateHCID 346961Methyl 6-chloro-5-nitronicotinateHCID 51758554-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acidHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 58324464
10-Oxo-1,3,4,9,10,10a-hexahydro-2,4-a,5,9-tetraaza-phenanthrene-2,7-dicarboxylic acid 2-tert-butyl ester 7-methyl ester

시약·촉매·용매 4

HCID 23939Platinum촉매HCID 62684Vanadic acid, ammonium salt촉매HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

실험 절차

To a suspension of 4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1169 mg, 5.08 mmol) in THF (46 mL) was added methyl 6-chloro-5-nitronicotinate (1000 mg, 4.62 mmol) and K2CO3 (638 mg, 4.62 mmol). The suspension was heated to reflux for 2 hours, cooled to room temperature, and filtered through a pad of celite. The celite was washed with DCM (50 mL) and the organic portions were combined. The solution was charged into a bomb hydroginator, then treated with triphenyl phosphite (0.015 ml, 0.048 mmol), ammonium vanadate (44 mg, 0.380 mmol), and platinum (1.853 g, 0.475 mmol). The reaction was sealed and pressurized with hydrogen gas (150 psi) overnight. The reaction was then diluted with DCM (100 mL) and heated to reflux for 1 hr. The hot mixture was filtered through celite, washed with DCM (50 mL), and concentrated to 1.65 g (96%) of the title compound as an off-white solid. [M+H] calc'd for C17H22N4O5, 363; found, 363.

후처리

  1. temperatureThe suspension was heated
  2. temperatureto reflux for 2 hours
  3. filtrationfiltered through a pad of celite
  4. washThe celite was washed with DCM (50 mL)
  5. additionThe solution was charged into a bomb hydroginator
  6. customThe reaction was sealed
  7. temperatureheated
  8. temperatureto reflux for 1 hr
  9. filtrationThe hot mixture was filtered through celite
  10. washwashed with DCM (50 mL)
  11. concentrationconcentrated to 1.65 g (96%) of the title compound as an off-white solid

출처 및 근거

ORD 기록
ord-6bde964455ed47ac8d17197c36cadb6a
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822470B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트