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Triethylamine → HCID 57884165, 화합물

HRID 1818084
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HRID 1818084 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10]([OH:12])=O)=[N:2]1.[CH3:13][O:14][C:15]1[CH:16]=[C:17]([C:23]2([CH2:28][NH2:29])[CH2:27][CH2:26][CH2:25][CH2:24]2)[CH:18]=[CH:19][C:20]=1[O:21][CH3:22].C(N(CC)CC)C.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1>C(#N)C>[CH3:13][O:14][C:15]1[CH:16]=[C:17]([C:23]2([CH2:28][NH:29][C:10]([C:3]3[C:4]4[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=4)[NH:1][N:2]=3)=[O:12])[CH2:24][CH2:25][CH2:26][CH2:27]2)[CH:18]=[CH:19][C:20]=1[O:21][CH3:22]
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 78250Indazole-3-carboxylic acidHCID 739193STK362959HCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)

생성물 1

HCID 57884165HCID 57884165, 화합물수율 9.9%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

1H-Indazole-3-carboxylic acid (32.4 mg, 0.200 mmol) and C-[1-(3,4-Dimethoxy-phenyl)-cyclopentyl]-methylamine (47.1 g, 0.200 mmol) were dissolved in acetonitrile (1 mL) containing triethylamine (83.6 μL, 0.600 mmol). O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (76.0 mg, 0.200 mmol) was added and the solution was allowed to stir for 16 hours. The mixture was then purified by reverse phase preparative liquid chromatography to yield the pure product (7.47 mg, 0.0197 mmol, 9.84%) ESI-MS m/z calc. 379.2, found 380.4 (M+1)+. Retention time of 3.02 minutes.

후처리

  1. customThe mixture was then purified by reverse phase preparative liquid chromatography

출처 및 근거

ORD 기록
ord-4abfe7cb665d4851b9355dcb2915821b
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07598412B2

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