HRID846984

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6809

Phthalimide

C8H5NO2

结构：CCCCCCCCCCCCCCCCCCNC(=O)OCC(CN)OC(=O)NC

HCID14834999

未命名化合物

HCID14992265

未命名化合物

结构：CCCCCCCCCCCCCCCCCCNC(=O)OCC(C)NC(=O)OC(C)(C)C

HCID19884226

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCCCCCCCCCCCC(=O)OCC(CN)NC(=O)OC(C)(C)C

HCID131717490

未命名化合物

PROCEDURE

实验过程

2-tert-Butoxycarbonylamino-3-octadecylcarbamoyloxypropane V e2 is allowed to react and worked up by the same procedure as described in (3). The phthalimide compound: m.p. 127°-129° C., The amino compound IV e2 69°-70° C. The summary of the experimental condition and the physical data of the product are listed in Tables 5 and 6.

WORKUP

后处理

customto react

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-73ae356a95f04ec99243e7972d7dbca4
来源数据集: uspto-grants-1992_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05138067
来源说明: uspto-grants-1992_08

反应 SMILES

[C:1]([O:5][C:6]([NH:8][CH:9]([CH2:11][O:12][C:13](=[O:33])NCCCCCCCCCCCCCCCCCC)[CH3:10])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(SCC(OC)C[NH2:54])CCCCCCCCCCCCCCC.C1(=O)NC(=O)C2=CC=CC=C12.CNC(OC(COC(=O)N[CH2:80][CH2:81][CH2:82][CH2:83][CH2:84][CH2:85][CH2:86][CH2:87][CH2:88][CH2:89][CH2:90][CH2:91][CH2:92][CH2:93][CH2:94][CH2:95][CH2:96][CH3:97])CN)=O>>[C:1]([O:5][C:6]([NH:8][CH:9]([CH2:11][O:12][C:13]([CH2:80][CH2:81][CH2:82][CH2:83][CH2:84][CH2:85][CH2:86][CH2:87][CH2:88][CH2:89][CH2:90][CH2:91][CH2:92][CH2:93][CH2:94][CH2:95][CH2:96][CH3:97])=[O:33])[CH2:10][NH2:54])=[O:7])([CH3:2])([CH3:3])[CH3:4]