Diisopropylethylamine → HCID 46909276, 화합물

HRID 1694313노트

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HRID 1694313 반응식
CCN(C(C)C)C(C)C.C1C=NC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl.[CH3:32][O:33][C:34]1[CH:35]=[C:36]2[C:41](=[CH:42][CH:43]=1)[CH:40]=[C:39]([S:44]([N:47]1[CH2:52][CH2:51][N:50]3[CH:53]=[CH:54][CH:55]=[C:49]3[CH:48]1[CH2:56][C:57](O)=[O:58])(=[O:46])=[O:45])[CH:38]=[CH:37]2.[N:60]1([CH2:66][C:67]2[CH:68]=[C:69]3[C:74](=[CH:75][CH:76]=2)[CH2:73][CH:72]([NH2:77])[CH2:71][CH2:70]3)[CH2:65][CH2:64][CH2:63][CH2:62][CH2:61]1>C(Cl)Cl>[CH3:32][O:33][C:34]1[CH:35]=[C:36]2[C:41](=[CH:42][CH:43]=1)[CH:40]=[C:39]([S:44]([N:47]1[CH2:52][CH2:51][N:50]3[CH:53]=[CH:54][CH:55]=[C:49]3[CH:48]1[CH2:56][C:57]([NH:77][CH:72]1[CH2:71][CH2:70][C:69]3[C:74](=[CH:75][CH:76]=[C:67]([CH2:66][N:60]4[CH2:65][CH2:64][CH2:63][CH2:62][CH2:61]4)[CH:68]=3)[CH2:73]1)=[O:58])(=[O:45])=[O:46])[CH:38]=[CH:37]2

참가 물질

7

실험 절차

DIPEA (2.5 eq.), HOAt (1.0 eq.) and EDCl (1.5 eq.) were added to a solution of 2-(2-(6-methoxynaphthalen-2-ylsulfonyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-1-yl)acetic acid S2 (0.2325 mmol, 1.0 eq.) in DCM (3 ml) at 0° C. and the mixture was stirred for 15 min at RT. Then 6-(piperidin-1-ylmethyl)-1,2,3,4-tetrahydronaphthalen-2-amine A5 (0.2325 mmol, 1.0 eq.) in DCM (2 ml) was added at 0° C. and the mixture was stirred overnight at RT. The reaction mixture was diluted with DCM and extracted with aqueous NaHCO3 solution, aqueous NH4Cl solution, water and saturated sodium chloride solution. The organic phase was dried (Na2SO4), concentrated to small volume and purified by column chromatography (alox). Yield: 58%; m/z=627.4 [MH]+

후처리

  1. extractionextracted with aqueous NaHCO3 solution, aqueous NH4Cl solution, water and saturated sodium chloride solution
  2. dry with materialThe organic phase was dried (Na2SO4)
  3. concentrationconcentrated to small volume
  4. custompurified by column chromatography (alox)

출처 및 근거

ORD 기록
ord-24401637caa449fa97e078cbec5ae423
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08158628B2

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