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Trifluoroacetic acid → HCID 178464158, 화합물

HRID 1919184
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HRID 1919184 반응식
CN(C(ON1N=N[C:11]2[CH:12]=[CH:13][CH:14]=N[C:10]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH2:25]([N:27]([CH2:38][CH3:39])[C@H:28]([C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[C:29](O)=[O:30])[CH3:26].[NH:40]1[CH2:44][CH2:43][CH2:42][C@H:41]1[C:45]1[NH:46][CH:47]=[C:48]([CH2:50][CH2:51][C:52]2[CH:57]=[CH:56][C:55]([CH2:58][CH2:59][C:60]3[NH:64][C:63]([C@@H:65]4[CH2:69][CH2:68][CH2:67][NH:66]4)=[N:62][CH:61]=3)=[CH:54][CH:53]=2)[N:49]=1.C(O)(C(F)(F)F)=[O:71].[CH3:77][CH2:78][N:79]([CH:83]([CH3:85])C)[CH:80]([CH3:82])[CH3:81]>CN(C=O)C.CO>[CH2:83]([N:79]([CH2:78][CH3:77])[C@H:80]([C:81]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:82]([N:66]1[CH2:67][CH2:68][CH2:69][C@H:65]1[C:63]1[NH:64][C:60]([CH2:59][CH2:58][C:55]2[CH:54]=[CH:53][C:52]([CH2:51][CH2:50][C:48]3[N:49]=[C:45]([C@@H:41]4[CH2:42][CH2:43][CH2:44][N:40]4[C:29](=[O:30])[C@@H:28]([C:32]4[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=4)[N:27]([CH2:38][CH3:39])[CH2:25][CH3:26])[NH:46][CH:47]=3)=[CH:57][CH:56]=2)=[CH:61][N:62]=1)=[O:71])[CH3:85]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 6422Trifluoroacetic acidHCID 81531DiisopropylethylamineHCID 1091378(R)-2-(diethylamino)-2-phenylacetic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 178420207HCID 178420207, 화합물

생성물 1

HCID 178464158
HCID 178464158, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 6228Dimethylformamide용매2회

실험 절차

HATU (76 mg, 0.2 mmole) was added to a stirred solution of (R)-2-(diethylamino)-2-phenylacetic acid (49 mg, 0.2 mmole) in DMF (1 mL) and DIEA (0.14 mL) and the mixture was stirred for 5 minutes. The 1-(2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)ethyl)-4-(2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)ethyl)benzene (40 mg) in DMF (1 mL) was added and the reaction mixture was stirred under argon for 16 hrs. The reaction mixture was purified directly by prep HPLC. The solid obtained, the TFA salt, was loaded onto an SCX ion exchange cartridge with methanol, then the product was isolated as the free base by eluting with a solution of 2 M NH3 in methanol to yield (1R)-2-((2S)-2-(4-(2-(4-(2-(2-((2S)-1-((2R)-2-(diethylamino)-2-phenylacetyl)-2-pyrrolidinyl)-1H-imidazol-5-yl)ethyl)phenyl)ethyl)-1H-imidazol-2-yl)-1-pyrrolidinyl)-N,N-diethyl-2-oxo-1-phenylethanamine (40 mg) as a white solid.

후처리

  1. stirringthe reaction mixture was stirred under argon for 16 hrs
  2. customThe reaction mixture was purified directly by prep HPLC
  3. customThe solid obtained
  4. customthe product was isolated as the free base
  5. washby eluting with a solution of 2 M NH3 in methanol

출처 및 근거

ORD 기록
ord-3d8b135d3fab49179fa8f38e79b3bec7
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618153B2

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