HRID2132360

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID679

Dimethyl sulfoxide

C2H6OS

HCID9886

Hexafluorophosphate ion

F6P-

HCID81531

Diisopropylethylamine

C8H19N

HCID5256896

2-(4-methyl-piperazin-1-ylmethyl)-piperidine

C11H23N3

结构：COC(N(C)c1ccccc1)=[N+](C(F)F)C(F)(F)F

HCID86594256

未命名化合物

结构：CC(Nc1ncnc2cc(C(=O)O)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1

HCID178463504

未命名化合物

PRODUCTS

生成物

结构：CC(Nc1ncnc2cc(C(=O)N3CCCCC3CN3CCN(C)CC3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1

HCID178463473

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-84c011b43acd43caaebc6bbb8149de25
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (4/10)

反应 SMILES

[CH3:63][N:64]1[CH2:65][CH2:66][N:67]([CH2:70][CH:71]2[NH:72][CH2:73][CH2:74][CH2:75][CH2:76]2)[CH2:68][CH2:69]1.[CH3:77][S:78]([CH3:79])=[O:80].[CH:54]([N:55]([CH:56]([CH3:57])[CH3:58])[CH2:59][CH3:60])([CH3:61])[CH3:62].[Cl:1][c:2]1[cH:3][c:4]2[c:5]([NH:15][CH:16]([CH3:17])[c:18]3[n:19][c:20]4[c:21]([nH:22]3)[cH:23][cH:24][c:25]([Cl:27])[cH:26]4)[n:6][cH:7][n:8][c:9]2[cH:10][c:11]1[C:12](=[O:13])[OH:14].[F:35][CH:36]([F:37])[N+:38]([C:39]([F:40])([F:41])[F:42])=[C:43]([N:44]([c:45]1[cH:46][cH:47][cH:48][cH:49][cH:50]1)[CH3:51])[O:52][CH3:53].[P-:28]([F:29])([F:30])([F:31])([F:32])([F:33])[F:34]>>[Cl:1][c:2]1[cH:3][c:4]2[c:5]([NH:15][CH:16]([CH3:17])[c:18]3[n:19][c:20]4[c:21]([nH:22]3)[cH:23][cH:24][c:25]([Cl:27])[cH:26]4)[n:6][cH:7][n:8][c:9]2[cH:10][c:11]1[C:12](=[O:13])[N:72]1[CH:71]([CH2:70][N:67]2[CH2:66][CH2:65][N:64]([CH3:63])[CH2:69][CH2:68]2)[CH2:76][CH2:75][CH2:74][CH2:73]1