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Hydrochloric Acid → N-[(1,2-Dihydro-2-methyl-1-oxo-4-phenylisoquinolin-3-yl)methyl]-N'-[3-(dimethylaminomethyl)phenyl]urea hydrochloride

HRID 260458
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HRID 260458 반응식
[CH3:1][N:2]1[C:11]([CH2:12]C(O)=O)=[C:10]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=[O:22].C1(P([N:37]=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[CH3:40][N:41]([CH2:43][C:44]1[CH:45]=[C:46]([CH:48]=[CH:49][CH:50]=1)[NH2:47])[CH3:42].[ClH:51].C([O:55][CH2:56]C)(=O)C>>[ClH:51].[CH3:1][N:2]1[C:11]([CH2:12][NH:37][C:56]([NH:47][C:46]2[CH:48]=[CH:49][CH:50]=[C:44]([CH2:43][N:41]([CH3:40])[CH3:42])[CH:45]=2)=[O:55])=[C:10]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=[O:22]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 992943-amino-N,N-dimethylbenzylamineHCID 199401P,P-Diphenylphosphinic azideHCID 104021291,2-Dihydro-2-methyl-1-oxo-4-phenyl-3-isoquinoline acetic acid

생성물 1

HCID 22401314
N-[(1,2-Dihydro-2-methyl-1-oxo-4-phenylisoquinolin-3-yl)methyl]-N'-[3-(dimethylaminomethyl)phenyl]urea hydrochloride

실험 절차

Using 1,2-dihydro-2-methyl-1-oxo-4-phenyl-3-isoquinoline acetic acid, diphenylphosphoryl azide and 3-(dimethylaminomethyl)aniline, the reaction was carried out by substantially the same procedure as in Method B of Example 1, followed by treatment of the product with hydrogen chloride in ethyl acetate to give the title compound as a white powdery product. NMR (200 MHz,DMSO-d6) ppm: 2.67(3H,s), 2.69(3H,s), 3.64(3H,s), 4.17(4H,m), 6.9-7.2(4H,m), 7.3-7.7(9H,m), 8.32(1H,m), 9.09(1H,bs)

출처 및 근거

ORD 기록
ord-20135b24567f494ca98b81410a796d51
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05527811

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