有机化学 ›› 2021, Vol. 41 ›› Issue (4): 1691-1702.DOI: 10.6023/cjoc202010023 上一篇 下一篇
研究论文
收稿日期:
2020-10-16
修回日期:
2020-11-11
发布日期:
2020-12-05
通讯作者:
程凯, 黄乐浩
基金资助:
Honglei Jina, Fengxuan Jiangb, Kai Chengb,*(), Lehao Huanga,*()
Received:
2020-10-16
Revised:
2020-11-11
Published:
2020-12-05
Contact:
Kai Cheng, Lehao Huang
About author:
Supported by:
文章分享
报道了一种钯催化1-萘酰胺的8位碳氢键烷基化反应. 在该反应中,喹啉甲酰胺作为N,N-双齿螯合基团, 各种取代的α-溴乙酸烷基酯以及α-溴代苯乙酮作为烷基化试剂, 高效、高区域选择性地合成了8-烷基-1-萘胺衍生物. 最后, 将含酯基和酮基的烷基化产物分别通过相应的衍生化反应合成具有多种生物活性的阿朴菲和马兜铃内酰胺类生物碱结构单元.
金红蕾, 姜风轩, 程凯, 黄乐浩. 钯催化1-萘酰胺的8-烷基化反应及其在阿朴菲和马兜铃内酰胺类生物碱骨架合成中的应用[J]. 有机化学, 2021, 41(4): 1691-1702.
Honglei Jin, Fengxuan Jiang, Kai Cheng, Lehao Huang. Palladium-Catalyzed C8 Alkylation of 1-Naphthylamides and Its Application to the Synthesis of the Core Sturctures of Aporphine and Aristolactam Alkaloids[J]. Chinese Journal of Organic Chemistry, 2021, 41(4): 1691-1702.
Entry | Catalyst/mol% | Additive | Solvent | Yieldb/% |
---|---|---|---|---|
1 | Pd(OAc)2 | KOAc | 1,4-Dioxane | 61 |
2 | Pd(OAc)2 | PhCOOK | 1,4-Dioxane | 68 |
3 | Pd(OAc)2 | PhCOOK | DMF | N.D. |
4 | Pd(OAc)2 | PhCOOK | Xylene | 82 |
5 | Pd(OAc)2 | PhCOOK | DMSO | N.D. |
6 | Pd(OAc)2 | PhCOOK | t-BuOH | 75 |
7 | Pd(OAc)2 | PhCOOK | DCE | 86 |
8 | Pd(OAc)2 | — | DCE | Trace |
9 | Pd(OAc)2 | AgOAc | DCE | Trace |
10 | Pd(OAc)2 | NaOAc | DCE | 49 |
11 | Pd(OAc)2 | K2CO3 | DCE | 45 |
12 | Pd(OAc)2 | Cs2CO3 | DCE | Trace |
13 | Pd(OAc)2 | HOAc | DCE | 18 |
14 | Pd(OAc)2 | CF3COOH | DCE | N.D. |
15 | PdCl2 | PhCOOK | DCE | 83 |
16 | Pd(PPh3)4 | PhCOOK | DCE | 36 |
17 | Pd2(dba)3 | PhCOOK | DCE | 30 |
18 | Pd(CH3CN)2Cl2 | PhCOOK | DCE | 80 |
Entry | Catalyst/mol% | Additive | Solvent | Yieldb/% |
---|---|---|---|---|
1 | Pd(OAc)2 | KOAc | 1,4-Dioxane | 61 |
2 | Pd(OAc)2 | PhCOOK | 1,4-Dioxane | 68 |
3 | Pd(OAc)2 | PhCOOK | DMF | N.D. |
4 | Pd(OAc)2 | PhCOOK | Xylene | 82 |
5 | Pd(OAc)2 | PhCOOK | DMSO | N.D. |
6 | Pd(OAc)2 | PhCOOK | t-BuOH | 75 |
7 | Pd(OAc)2 | PhCOOK | DCE | 86 |
8 | Pd(OAc)2 | — | DCE | Trace |
9 | Pd(OAc)2 | AgOAc | DCE | Trace |
10 | Pd(OAc)2 | NaOAc | DCE | 49 |
11 | Pd(OAc)2 | K2CO3 | DCE | 45 |
12 | Pd(OAc)2 | Cs2CO3 | DCE | Trace |
13 | Pd(OAc)2 | HOAc | DCE | 18 |
14 | Pd(OAc)2 | CF3COOH | DCE | N.D. |
15 | PdCl2 | PhCOOK | DCE | 83 |
16 | Pd(PPh3)4 | PhCOOK | DCE | 36 |
17 | Pd2(dba)3 | PhCOOK | DCE | 30 |
18 | Pd(CH3CN)2Cl2 | PhCOOK | DCE | 80 |
Entry | α-Bromo ketones | Product | Yieldb/% | Entry | α-Bromo ketones | Product | Yieldb/% |
---|---|---|---|---|---|---|---|
1 | | 3f | 82 (74c) | 6 | | 3k | 70 |
2 | | 3g | 79 | 7 | | 3l | 78 |
3 | | 3h | 64 | 8 | | 3m | 71 |
4 | | 3i | 55 | 9 | | 3n | 52 |
5 | | 3j | 76 | 10d | | 3o | 56 |
Entry | α-Bromo ketones | Product | Yieldb/% | Entry | α-Bromo ketones | Product | Yieldb/% |
---|---|---|---|---|---|---|---|
1 | | 3f | 82 (74c) | 6 | | 3k | 70 |
2 | | 3g | 79 | 7 | | 3l | 78 |
3 | | 3h | 64 | 8 | | 3m | 71 |
4 | | 3i | 55 | 9 | | 3n | 52 |
5 | | 3j | 76 | 10d | | 3o | 56 |
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