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4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride → HCID 49806037, 화합물

HRID 576887
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HRID 576887 반응식
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C@H:16]([N:20]([CH3:37])[NH:21][C:22](=[O:36])[CH2:23][CH2:24][NH:25][C:26]([NH:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)=[O:27])[C:17]([OH:19])=O)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:38]([O:40][CH:41]([O:55][CH2:56][CH3:57])[CH2:42][NH:43][CH2:44][C:45]1[C:54]2[C:49](=[CH:50][CH:51]=[CH:52][CH:53]=2)[CH:48]=[CH:47][CH:46]=1)[CH3:39].C[N+]1(C2N=C(OC)N=C(OC)N=2)CCOCC1.[Cl-]>ClCCl.C(Cl)(Cl)Cl>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:15][C@H:16]([N:20]([CH3:37])[NH:21][C:22](=[O:36])[CH2:23][CH2:24][NH:25][C:26]([NH:28][CH2:29][C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=2)=[O:27])[C:17]([N:43]([CH2:42][CH:41]([O:40][CH2:38][CH3:39])[O:55][CH2:56][CH3:57])[CH2:44][C:45]2[C:54]3[C:49](=[CH:50][CH:51]=[CH:52][CH:53]=3)[CH:48]=[CH:47][CH:46]=2)=[O:19])=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 27340594-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 53411263HCID 53411263, 화합물HCID 66644546HCID 66644546, 화합물

생성물 1

HCID 49806037HCID 49806037, 화합물수율 44.7%

시약·촉매·용매 2

HCID 6212Chloroform용매
HCID 6344
Dichloromethane
용매

실험 절차

To a solution of (S)-3-(4-(benzyloxy)phenyl)-2-(2-(3-(3-benzylureido)propanoyl)-1-methylhydrazinyl)propanoic acid (Compound VII-1) 126 mg (0.25 mmol) in dichloromethane 1.5 ml, 2,2-diethoxy-N-(naphthalen-1-ylmethyl)ethanamine (Compound IV-2) 85 mg (0.31 mmol) and DMT-MM 173 mg (0.63 mmol) were added and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with chloroform 50 ml and washed with water 50 ml twice and brine 50 ml twice and dried over magnesium sulfate and filtered. The mother solution was concentrated in vacuo and the residue was purified on silica gel column chromatography (Merck 60N spherical, neutral 10 ml elution by chloroform:methanol=100:0 to 90:10, each elution 50 ml) to give the desired product as pale yellow oil 85.0 mg (35.8%).

후처리

  1. washwashed with water 50 ml twice
  2. dry with materialbrine 50 ml twice and dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationThe mother solution was concentrated in vacuo
  5. customthe residue was purified on silica gel column chromatography (Merck 60N spherical
  6. washneutral 10 ml elution by chloroform
  7. washmethanol=100:0 to 90:10, each elution 50 ml)

출처 및 근거

ORD 기록
ord-8fda5ffcc2eb4998b6756fe0ccb320b4
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040531B2

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