JP2012519194A5 - - Google Patents
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- Publication number
- JP2012519194A5 JP2012519194A5 JP2011552321A JP2011552321A JP2012519194A5 JP 2012519194 A5 JP2012519194 A5 JP 2012519194A5 JP 2011552321 A JP2011552321 A JP 2011552321A JP 2011552321 A JP2011552321 A JP 2011552321A JP 2012519194 A5 JP2012519194 A5 JP 2012519194A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- aryl
- group
- chiral
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 NH 2 Inorganic materials 0.000 claims 13
- 239000002184 metal Chemical class 0.000 claims 13
- 229910052751 metal Inorganic materials 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 13
- 125000003118 aryl group Chemical group 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 11
- 238000000034 method Methods 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 230000008569 process Effects 0.000 claims 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 6
- 125000005842 heteroatom Chemical group 0.000 claims 6
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 claims 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 150000003949 imides Chemical class 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 4
- 150000001299 aldehydes Chemical class 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 150000002576 ketones Chemical class 0.000 claims 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 2
- 125000006649 (C2-C20) alkynyl group Chemical group 0.000 claims 2
- PPTXVXKCQZKFBN-UHFFFAOYSA-N (S)-(-)-1,1'-Bi-2-naphthol Chemical compound C1=CC=C2C(C3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 PPTXVXKCQZKFBN-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 239000007848 Bronsted acid Substances 0.000 claims 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 2
- 238000003799 Mukaiyama Aldol addition reaction Methods 0.000 claims 2
- 238000005575 aldol reaction Methods 0.000 claims 2
- 150000001336 alkenes Chemical class 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims 2
- 239000011968 lewis acid catalyst Substances 0.000 claims 2
- 229910052744 lithium Inorganic materials 0.000 claims 2
- 229910052749 magnesium Inorganic materials 0.000 claims 2
- 238000007142 ring opening reaction Methods 0.000 claims 2
- 229910052725 zinc Inorganic materials 0.000 claims 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 1
- 125000004361 3,4,5-trifluorophenyl group Chemical group [H]C1=C(F)C(F)=C(F)C([H])=C1* 0.000 claims 1
- GGUOCFNAWIODMF-UHFFFAOYSA-N 4-chloroacetanilide Chemical compound CC(=O)NC1=CC=C(Cl)C=C1 GGUOCFNAWIODMF-UHFFFAOYSA-N 0.000 claims 1
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 claims 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 claims 1
- 238000006683 Mannich reaction Methods 0.000 claims 1
- 238000006845 Michael addition reaction Methods 0.000 claims 1
- 238000003687 Mukaiyama-Michael addition reaction Methods 0.000 claims 1
- 238000010475 Pinacol rearrangement reaction Methods 0.000 claims 1
- 238000006359 acetalization reaction Methods 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 230000004913 activation Effects 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 238000005865 alkene metathesis reaction Methods 0.000 claims 1
- 150000001345 alkine derivatives Chemical class 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 238000005937 allylation reaction Methods 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- NBYQXBYMEUOBON-UHFFFAOYSA-N carbamothioyl chloride Chemical compound NC(Cl)=S NBYQXBYMEUOBON-UHFFFAOYSA-N 0.000 claims 1
- 238000006555 catalytic reaction Methods 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- VXRUJZQPKRBJKH-UHFFFAOYSA-N corannulene Chemical compound C1=CC(C2=C34)=CC=C3C=CC3=C4C4=C2C1=CC=C4C=C3 VXRUJZQPKRBJKH-UHFFFAOYSA-N 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 238000006352 cycloaddition reaction Methods 0.000 claims 1
- 239000012039 electrophile Substances 0.000 claims 1
- 150000002081 enamines Chemical class 0.000 claims 1
- 238000006735 epoxidation reaction Methods 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 238000006266 etherification reaction Methods 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 230000036571 hydration Effects 0.000 claims 1
- 238000006703 hydration reaction Methods 0.000 claims 1
- 238000005913 hydroamination reaction Methods 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 238000006317 isomerization reaction Methods 0.000 claims 1
- REWJFHAZUPISFU-UHFFFAOYSA-N n-(2,3,4,5,6-pentafluorophenyl)acetamide Chemical compound CC(=O)NC1=C(F)C(F)=C(F)C(F)=C1F REWJFHAZUPISFU-UHFFFAOYSA-N 0.000 claims 1
- FBMIRBWQIPKRAB-UHFFFAOYSA-N n-[2,6-di(propan-2-yl)phenyl]acetamide Chemical compound CC(C)C1=CC=CC(C(C)C)=C1NC(C)=O FBMIRBWQIPKRAB-UHFFFAOYSA-N 0.000 claims 1
- WEASGADRJWKQRE-UHFFFAOYSA-N n-benzhydrylacetamide Chemical compound C=1C=CC=CC=1C(NC(=O)C)C1=CC=CC=C1 WEASGADRJWKQRE-UHFFFAOYSA-N 0.000 claims 1
- OKQIEBVRUGLWOR-UHFFFAOYSA-N n-naphthalen-1-ylacetamide Chemical compound C1=CC=C2C(NC(=O)C)=CC=CC2=C1 OKQIEBVRUGLWOR-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 238000010534 nucleophilic substitution reaction Methods 0.000 claims 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
- 150000002894 organic compounds Chemical class 0.000 claims 1
- 239000007800 oxidant agent Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims 1
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- 150000004032 porphyrins Chemical class 0.000 claims 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims 1
- 230000009467 reduction Effects 0.000 claims 1
- 239000003579 shift reagent Substances 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 238000009901 transfer hydrogenation reaction Methods 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 claims 1
- 0 C*S(c1c(*)c(*)c(C(*)(*I)C(C)(*)C(C)(*)C2(C)*)c2c1-c1c(C(C)(*)C(C)(*)*(C)C2(*)*)c2c(*)c(*)c1C)(=*)=O Chemical compound C*S(c1c(*)c(*)c(C(*)(*I)C(C)(*)C(C)(*)C2(C)*)c2c1-c1c(C(C)(*)C(C)(*)*(C)C2(*)*)c2c(*)c(*)c1C)(=*)=O 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009011055A DE102009011055A1 (de) | 2009-03-02 | 2009-03-02 | Chirale Disulfonsäuren und Disulfonimide |
| DE102009011055.0 | 2009-03-02 | ||
| PCT/DE2010/000226 WO2010099786A1 (de) | 2009-03-02 | 2010-03-02 | Chirale disulfonimide |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012519194A JP2012519194A (ja) | 2012-08-23 |
| JP2012519194A5 true JP2012519194A5 (enExample) | 2013-02-07 |
| JP5738204B2 JP5738204B2 (ja) | 2015-06-17 |
Family
ID=42289514
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011552321A Active JP5738204B2 (ja) | 2009-03-02 | 2010-03-02 | キラルなジスルホンイミド |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9079869B2 (enExample) |
| EP (1) | EP2403842B1 (enExample) |
| JP (1) | JP5738204B2 (enExample) |
| CA (1) | CA2754298C (enExample) |
| DE (1) | DE102009011055A1 (enExample) |
| ES (1) | ES2593854T3 (enExample) |
| WO (1) | WO2010099786A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113461589B (zh) * | 2021-07-27 | 2022-10-14 | 上海工程技术大学 | 一种手性2，3-二取代吲哚胺类化合物及其制备方法 |
| CN115155658B (zh) * | 2022-09-06 | 2022-11-25 | 泽升科技(广州)有限公司 | 一类基于vapol合成硒硫类化合物的合成方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2001307A (en) * | 1977-07-01 | 1979-01-31 | American Cyanamid Co | Sulphonamide blood complement inhibitors |
| US4122088A (en) | 1977-07-01 | 1978-10-24 | American Cyanamid Company | Dicarboxyphenyl substituted bis-sulfonylimino dibenzodithiazepine tetroxides |
| JP2005134365A (ja) | 2003-10-07 | 2005-05-26 | Sumitomo Chemical Co Ltd | 光学活性ビナフチル化合物からなるｎｍｒ用キラルシフト試薬 |
| JP2005132816A (ja) | 2003-10-07 | 2005-05-26 | Sumitomo Chemical Co Ltd | 光学活性ビナフチル化合物からなる光学分割試薬 |
| JP2005132815A (ja) | 2003-10-07 | 2005-05-26 | Sumitomo Chemical Co Ltd | 光学活性スルホン酸化合物 |
| JP2010111661A (ja) * | 2008-10-09 | 2010-05-20 | Sumitomo Chemical Co Ltd | 芳香族スルホニルクロリドおよび芳香族スルホン酸化合物の製造方法、並びに芳香族スルホン酸化合物およびその製造中間体 |
-
2009
- 2009-03-02 DE DE102009011055A patent/DE102009011055A1/de not_active Withdrawn
-
2010
- 2010-03-02 CA CA2754298A patent/CA2754298C/en active Active
- 2010-03-02 ES ES10714559.1T patent/ES2593854T3/es active Active
- 2010-03-02 EP EP10714559.1A patent/EP2403842B1/de active Active
- 2010-03-02 JP JP2011552321A patent/JP5738204B2/ja active Active
- 2010-03-02 US US13/203,382 patent/US9079869B2/en active Active
- 2010-03-02 WO PCT/DE2010/000226 patent/WO2010099786A1/de not_active Ceased
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