HRID2403837

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCCCOc1nc(N)c2nc(OC)n(CCCC3CCCCN3C(=O)OCc3ccccc3)c2n1

HCID58306132

未命名化合物

HCID58306229

未命名化合物

结构：CCCCOc1nc(N)c2nc(OC)[nH]c2n1.O=C(O)C(F)(F)F

HCID178450370

未命名化合物

PRODUCTS

生成物

结构：CCCCOc1nc(N)c2nc(OC)n(CCCCCC3CCCN(C(=O)OCc4ccccc4)C3)c2n1

HCID58306261

未命名化合物

PROCEDURE

实验过程

Prepared similarly to Intermediate 31 from 2-(butyloxy)-8-(methyloxy)-9H-purin-6-amine trifluoroacetate and phenylmethyl 3-(5-bromopentyl)-1-piperidinecarboxylate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-79c90579bbe94b3aa54a0f8cb3b0afba
来源数据集: uspto-grants-2014_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08802684B2
来源说明: uspto-grants-2014_08

反应 SMILES

[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([O:35][CH3:36])[N:6]2[CH2:16][CH2:17][CH2:18][CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21]N1C(OCC1C=CC=CC=1)=O.FC(F)(F)C(O)=O.C(OC1N=C2C(N=C(OC)N2)=C(N)N=1)CCC.BrCCCCCC1CC[CH2:70][N:69]([C:73]([O:75][CH2:76][C:77]2[CH:82]=[CH:81][CH:80]=[CH:79][CH:78]=2)=[O:74])[CH2:68]1>>[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([O:35][CH3:36])[N:6]2[CH2:16][CH2:17][CH2:18][CH2:19][CH2:24][CH:23]1[CH2:22][CH2:21][CH2:68][N:69]([C:73]([O:75][CH2:76][C:77]2[CH:82]=[CH:81][CH:80]=[CH:79][CH:78]=2)=[O:74])[CH2:70]1