HRID1218914

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID13831

Tributylphosphine

C12H27P

HCID73042

1,1′-(1,2-Diazenediyl)bis[1-(1-piperidinyl)methanone]

C12H20N4O2

HCID518900

Methyl (4-hydroxyphenyl)acetate

C9H10O3

结构：Cc1nccn1-c1nc(-c2ccc(Cl)cc2)c(CCCO)o1

HCID9926997

4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol

C16H16ClN3O2

PRODUCTS

生成物

结构：COC(=O)Cc1ccc(OCCCc2oc(-n3ccnc3C)nc2-c2ccc(Cl)cc2)cc1

HCID18174741

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d84a9c3264034a4abe23742d2e6b8582
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (5/10)

反应 SMILES

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