JP2018057390A5 - - Google Patents

Info

Publication number

JP2018057390A5

JP2018057390A5 JP2017220693A JP2017220693A JP2018057390A5 JP 2018057390 A5 JP2018057390 A5 JP 2018057390A5 JP 2017220693 A JP2017220693 A JP 2017220693A JP 2017220693 A JP2017220693 A JP 2017220693A JP 2018057390 A5 JP2018057390 A5 JP 2018057390A5

Authority

JP

Japan

Prior art keywords

carboxamide

smoking article

menthane

article according

inclusion complex

Prior art date

2017-11-16

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.)

Pending

Links

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• 230000000391 smoking effect Effects 0.000 claims 15
• 239000003795 chemical substances by application Substances 0.000 claims 10
• 150000001875 compounds Chemical class 0.000 claims 10
• 150000003857 carboxamides Chemical group 0.000 claims 7
• 229920000858 Cyclodextrin Polymers 0.000 claims 6
• HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical group O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims 6
• 125000000217 alkyl group Chemical group 0.000 claims 4
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
• 125000003545 alkoxy group Chemical group 0.000 claims 3
• 238000000034 method Methods 0.000 claims 3
• VUNOFAIHSALQQH-UHFFFAOYSA-N Ethyl menthane carboxamide Chemical compound CCNC(=O)C1CC(C)CCC1C(C)C VUNOFAIHSALQQH-UHFFFAOYSA-N 0.000 claims 2
• RWAXQWRDVUOOGG-UHFFFAOYSA-N N,2,3-Trimethyl-2-(1-methylethyl)butanamide Chemical compound CNC(=O)C(C)(C(C)C)C(C)C RWAXQWRDVUOOGG-UHFFFAOYSA-N 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 claims 1
• HNSGVPAAXJJOPQ-XOKHGSTOSA-N (1r,2s,5r)-n-(4-methoxyphenyl)-5-methyl-2-propan-2-ylcyclohexane-1-carboxamide Chemical compound C1=CC(OC)=CC=C1NC(=O)[C@H]1[C@H](C(C)C)CC[C@@H](C)C1 HNSGVPAAXJJOPQ-XOKHGSTOSA-N 0.000 claims 1
• -1 1-isopropyl-1-methylisobutyl Chemical group 0.000 claims 1
• FVBGFZNFXUIHNC-GRYCIOLGSA-N 2-[(1r,2s,5r)-5-methyl-2-propan-2-ylcyclohexyl]oxyethanol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OCCO FVBGFZNFXUIHNC-GRYCIOLGSA-N 0.000 claims 1
• MDVYIGJINBYKOM-UHFFFAOYSA-N 3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]-1,2-propanediol Chemical compound CC(C)C1CCC(C)CC1OCC(O)CO MDVYIGJINBYKOM-UHFFFAOYSA-N 0.000 claims 1
• WHBMMWSBFZVSSR-UHFFFAOYSA-M 3-hydroxybutyrate Chemical compound CC(O)CC([O-])=O WHBMMWSBFZVSSR-UHFFFAOYSA-M 0.000 claims 1
• WAIGPJMZARQZDX-UHFFFAOYSA-N 4-(dimethylamino)-4-oxobutanoic acid Chemical compound CN(C)C(=O)CCC(O)=O WAIGPJMZARQZDX-UHFFFAOYSA-N 0.000 claims 1
• GUCPYIYFQVTFSI-UHFFFAOYSA-N 4-methoxybenzamide Chemical compound COC1=CC=C(C(N)=O)C=C1 GUCPYIYFQVTFSI-UHFFFAOYSA-N 0.000 claims 1
• CTMTYSVTTGVYAW-FRRDWIJNSA-N 5-[(1r,2s,5r)-5-methyl-2-propan-2-ylcyclohexyl]oxy-5-oxopentanoic acid Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)CCCC(O)=O CTMTYSVTTGVYAW-FRRDWIJNSA-N 0.000 claims 1
• LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 1
• LMXFTMYMHGYJEI-UHFFFAOYSA-N Menthoglycol Natural products CC1CCC(C(C)(C)O)C(O)C1 LMXFTMYMHGYJEI-UHFFFAOYSA-N 0.000 claims 1
• NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 claims 1
• BLILOGGUTRWFNI-UHFFFAOYSA-N Monomenthyl succinate Chemical compound CC(C)C1CCC(C)CC1OC(=O)CCC(O)=O BLILOGGUTRWFNI-UHFFFAOYSA-N 0.000 claims 1
• GWRCTWAPTXBPHW-UHFFFAOYSA-N N-[(Ethoxycarbonyl)methyl)-p-menthane-3-carboxamide Chemical compound CCOC(=O)CNC(=O)C1CC(C)CCC1C(C)C GWRCTWAPTXBPHW-UHFFFAOYSA-N 0.000 claims 1
• WHBMMWSBFZVSSR-UHFFFAOYSA-N R3HBA Natural products CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 claims 1
• UJNOLBSYLSYIBM-WISYIIOYSA-N [(1r,2s,5r)-5-methyl-2-propan-2-ylcyclohexyl] (2r)-2-hydroxypropanoate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)[C@@H](C)O UJNOLBSYLSYIBM-WISYIIOYSA-N 0.000 claims 1
• 125000000732 arylene group Chemical group 0.000 claims 1
• 239000002826 coolant Substances 0.000 claims 1
• 150000002148 esters Chemical class 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 229930007503 menthone Natural products 0.000 claims 1
• PCOMMNVANAQDMV-UHFFFAOYSA-N n,2-diethyl-3-methyl-2-propan-2-ylbutanamide Chemical compound CCNC(=O)C(CC)(C(C)C)C(C)C PCOMMNVANAQDMV-UHFFFAOYSA-N 0.000 claims 1
• PMLXIBABNSSOID-UHFFFAOYSA-N n-(2-ethoxyethyl)-2,3-dimethyl-2-propan-2-ylbutanamide Chemical compound CCOCCNC(=O)C(C)(C(C)C)C(C)C PMLXIBABNSSOID-UHFFFAOYSA-N 0.000 claims 1
• CUNIMRNZTKYNGN-UHFFFAOYSA-N n-(2-hydroxyethyl)-2,3-dimethyl-2-propan-2-ylbutanamide Chemical compound CC(C)C(C)(C(C)C)C(=O)NCCO CUNIMRNZTKYNGN-UHFFFAOYSA-N 0.000 claims 1
• FPJRGEOLQICYQZ-UHFFFAOYSA-N n-[4-(cyanomethyl)phenyl]-5-methyl-2-propan-2-ylcyclohexane-1-carboxamide Chemical compound CC(C)C1CCC(C)CC1C(=O)NC1=CC=C(CC#N)C=C1 FPJRGEOLQICYQZ-UHFFFAOYSA-N 0.000 claims 1
• 125000004076 pyridyl group Chemical group 0.000 claims 1
• UJNOLBSYLSYIBM-UHFFFAOYSA-N CC(C)C(CCC(C)C1)C1OC(C(C)O)=O Chemical compound CC(C)C(CCC(C)C1)C1OC(C(C)O)=O UJNOLBSYLSYIBM-UHFFFAOYSA-N 0.000 description 1