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

1,10-Phenanthroline → HCID 178454064, 화합물

HRID 1041905
노트
인쇄 미리보기

반응식

HRID 1041905 반응식
I[C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:8]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH2:18][CH2:19][N:20]4[CH2:25][CH2:24][O:23][CH2:22][CH2:21]4)[CH:12]=3)=[N:9][N:10]=2)[CH:7]=1.N1C2C(=CC=C3C=2N=CC=C3)C=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:46][C:47]([O:50][C:51]([NH:53][CH:54]1[CH2:59][CH2:58][CH:57]([OH:60])[CH2:56][CH2:55]1)=[O:52])([CH3:49])[CH3:48]>C1(C)C=CC=CC=1.CCOC(C)=O.[Cu]I>[C:47]([O:50][C:51](=[O:52])[NH:53][C@H:54]1[CH2:55][CH2:56][C@H:57]([O:60][C:2]2[CH:3]=[CH:4][C:5]3[N:6]([C:8]([C:11]4[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH2:18][CH2:19][N:20]5[CH2:25][CH2:24][O:23][CH2:22][CH2:21]5)[CH:12]=4)=[N:9][N:10]=3)[CH:7]=2)[CH2:58][CH2:59]1)([CH3:49])([CH3:46])[CH3:48]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 13181,10-PhenanthrolineHCID 10796Cesium carbonateHCID 1514287cis-4-(tert-Butoxycarbonylamino)cyclohexanolHCID 669775456-Iodo-3-[3-(2-morpholin-4-yl-ethoxy)-phenyl]-[1,2,4]triazolo[4,3-a]pyridine

생성물 1

HCID 178454064HCID 178454064, 화합물수율 73.3%

시약·촉매·용매 3

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
촉매
HCID 1140Toluene용매
HCID 8857Ethyl Acetate용매

실험 절차

A mixture of Example 1 step b (234 mg, 0.52 mmol), copper (I) iodide (9 mg, 0.052 mmol), 1,10-phenanthroline (19 mg, 0.104 mmol), cesium carbonate (335 mg, 1.04 mmol) and trans-4-boc-aminocyclohexanol (560 mg, 2.6 mmol) in toluene (3 mL) was heated at 110° C. for 72 h under an argon atmosphere. The suspension was cooled to RT, diluted with EtOAc (10 mL) and filtered through HiFlo. The filtrate was concentrated in vacuo and the residue purified by reverse phase preparative HPLC (Method 3) to afford the title compound (205 mg, 39%) as an off-white solid. LCMS (Method 2): Rt 2.53 min, m/z 538 [MH+].

후처리

  1. filtrationfiltered through HiFlo
  2. concentrationThe filtrate was concentrated in vacuo
  3. customthe residue purified by reverse phase preparative HPLC (Method 3)

출처 및 근거

ORD 기록
ord-c00f5bfe70e341b997c8ca8b566c3676
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557797B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트