JP2021511378A - 新たなスピロオキサチオラノン化合物、その調製方法、ならびに香料製造および芳香化合物におけるその使用 - Google Patents
新たなスピロオキサチオラノン化合物、その調製方法、ならびに香料製造および芳香化合物におけるその使用 Download PDFInfo
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- JP2021511378A JP2021511378A JP2020560573A JP2020560573A JP2021511378A JP 2021511378 A JP2021511378 A JP 2021511378A JP 2020560573 A JP2020560573 A JP 2020560573A JP 2020560573 A JP2020560573 A JP 2020560573A JP 2021511378 A JP2021511378 A JP 2021511378A
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- oxa
- thiaspiro
- decan
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/04—Five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
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- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
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Abstract
Description
−R1、R2、R3、R4、R6およびR7は、独立して水素原子またはメチル基を表し;
−R5は、水素原子または飽和直鎖C1〜C5アルキル基を表し;
−R4およびR5は、一緒になってシクロペンチル基を形成することができ;
−炭素原子の総数は、厳密に9より大きい。
−R1、R2、R3、R4、R6およびR7は、独立して水素原子またはメチル基を表し;
−R5は、水素原子または飽和直鎖C1〜C5アルキル基を表し;
−R4およびR5は、一緒になってシクロペンチル基を形成することができ;
−炭素原子の総数は、厳密に9より大きい。
−R1、R2、R3、R4、R6およびR7は、独立して水素原子またはメチル基を表し;
−R5は、水素原子または飽和直鎖C1〜C5アルキル基を表し;
−R4およびR5は、一緒になってシクロペンチル基を形成することができ;
−炭素原子の総数は、厳密に9より大きい。
−R1、R2、R3、R4、R6およびR7は、独立して水素原子またはメチル基を表し;
−R5は、水素原子または飽和直鎖C1〜C5アルキル基を表し;
−R4およびR5は、一緒になってシクロペンチル基を形成することができ;
−炭素原子の総数は、厳密に9より大きい。
第1の実施形態において、式(I)の少なくとも1種の化合物は、少なくとも1種の他の香気物質および/または少なくとも1種の溶媒および/または少なくとも1種の添加剤と組み合わせた、または個別の香味剤として使用される。追加の香気剤、溶媒および添加剤は、求められる効果に従って最も適切なものを選択することができる当業者に知られている。
1H−RMN(300MHz、CDCl3):δ(ppm)3,73(s,1H)、3.72(s,1H)、2.10−1.90(m,2H)、1.85−1.58(m、4H)、1.46−1.29(m,1H)、1.34−1.16(m,1H)、1.04(s,3H)、0.97(s,3H)。
13C−RMN(75MHz、CDCl3):δ(ppm)172.34、92.16、51.31、39.82、37.74、32.23、31.11、28.37、19.90。
SM[EI+](m/z)(%):200(M+,9)、127(100)、109(55)、83(25)、69(34)、56(10)、55(35)、46(12)、43(26)、41(25)、39(10)。
IR(pure,cm−1):2946m、1765s、1455w、1215m、1144m、1060m、1025m、993m、954m、914w、811w、797w、607w。
1H−RMN(300MHz,CDCl3):δ(ppm)3.62(s,2H),2.21−2.06(m,1H),2.05−1.88(m,2H),1.80−1.60(m,3H),1.40−1.23(m,1H),1.26−1.04(m,4H),0.81(td,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.24,94.34,38.70,37.43,31.69,39.34,11.57.
SM[EI+](m/z)(%):200(M+,10),127(100),109(37),67(33),55(41),46(12),43(13),41(22).
1H−RMN(300MHz,CDCl3):δ(ppm)3.69(s,2H),2.21−2.06(m,1H),2.05−1.88(m,2H),1.80−1.60(m,3H),1.40−1.23(m,1H),1.26−1.04(m,4H),0.81(td,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.26,91.48,39.49,37.17,32.25,29.12,28.69,11.47.
SM[e/m(%)]:200(M+,10),129(10),127(100),109(35),67(33),55(42),46(12),43(14),41(23).
IR(pure,cm−1):2926m,1767s,1442w,1197m,1139m,1041m,966m,915w,892w,854w,796w.
1H−RMN(300MHz,CDCl3):δ(ppm)3.99(q,J=7.0Hz,1H),2.28−2.09(m,1H),2.09−1.61(m,5H),1.57(d,J=7.0Hz,3H),1.52−0.95(m,5H),0.88(t,J=7.0Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)175.19,91.63,40.90,39.61,38.96,37.52,29.78,29.15,28.71,18.40,11.60.
SM[EI+](m/z)(%):210(M+,0.3),195(100),137(24),109(34),101(998),93(10),91(14),81(11),79(15),76(15),67(16),43(64),41(16).
1H−RMN(300MHz,CDCl3):δ(ppm)3.99(q,J=7.0Hz,1H),2.28−2.09(m,1H),2.09−1.61(m,5H),1.58(d,J=7.0Hz,3H),1.52−0.95(m,5H),0.87(t,J=7.0Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)175.25,88.74,41.43,40.27,39.74,37.28,29.23,29.06,28.76,18.54,11.50.
SM[EI+](m/z)(%):214[M+](6),127(100),109(19),67(12),60(20),55(23),41(15).
IR(film,cm−1):1039m,1209m,1447s,1761s,2928m.
1H−RMN(300MHz,CDCl3):δ(ppm)3.71(s,2H),2.19−2.01(m,2H),1.98−1.80(m,2H),1.63−1.30(m,4H),0.94(2s,6H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.35,93.19,36.05,35.74,31.95,29.11.
SM[EI+](m/z)(%):200(M+,12),127(100),109(35),71(15),67(16),55(33),46(15),43(24),41(24),39(10).
IR(pure,cm−1):2950m,1767s,1444w,1232m,1215m,1156m,1045s,1001m,972m,877m,791w,585w.
1H−RMN(300MHz,CDCl3):δ(ppm)3.74(s,2H),2.22−2.16(m,1H),2.05−1.95(m,2H),1.85−1.64(m,3H),1.40−1.11(m,7H),0.89−0.84(t,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.38,94.50,38.79,38.27,31.78,29.73,20.12,14.27.
SM[EI+](m/z)(%):214(M+,7),142(10),141(100),81(43),67(20),55(28),46(10),43(10),41(18).
1H−RMN(300MHz,CDCl3):δ(ppm)3.68(s,2H),2.22−2.16(m,1H),2.05−1.95(m,2H),1.85−1.64(m,3H),1.40−1.11(m,7H),0.89−0.84(t,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.38,91.65,39.58,38.24,32.24,29.50,20.00,14.27.
MS[e/m(%)]:214(M+,9),141(100),81(39),67(19),55(22),41(15).
IR(pure,cm−1):2926m,1768s,1443w,1223m,1193m,1137w,1043m,969m,912w,842w,796w,589w.
1H−RMN(300MHz,CDCl3):δ(ppm)3.98(q,J=7.0Hz,1H),2.26−1.61(m,6H),1.56(d,J=7.0Hz,3H),1.51−0.95(m,7H),0.87(t,J=7.0Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)175.12,91.56,41.39,40.86,39.60,38.95,38.25,35.48,30.12,20.11,18.38,14.26.
SM[EI+](m/z)(%):228[M+](3),142(10),141(100),81(20),67(10)
1H−RMN(300MHz,CDCl3):δ(ppm)4.06(q,J=7.0Hz,1H),2.26−1.61(m,6H),1.57(d,J=7.0Hz,3H),1.51−0.95(m,7H),0.86(t,J=7.0Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)175.18,88.68,41.39,40.24,39.73,38.30,35.22,29.56,29.40,19.99,18.52,14.26.
SM[EI+](m/z)(%):228[M+](3),142(10),141(100),81(20),67(10),60(13)
IR(フィルム、cm−1):1036m、1224m、1443m、1755s、1926m。
1H−RMN(300MHz,CDCl3):(ppm)3.74(s,2H),2.16−2.07(m,2H),1.97−1.88(m,2H),1.69−1.59(m,6H),1.54−1.43(m,6H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.42,93.38,41.20,37.02,34.68,32.00,24.45,24.39.
SM[EI+](m/z)(%):226(M+,6),154(11),153(100),135(10),67(14),55(15).
IR(pure,cm−1):2943m,1771s,1443m,1267m,1221s,1209s,1131m,1041s,978m,933m,900w,838m,794m,608w.
1H−RMN(300MHz,CDCl3):δ(ppm)3.73(s,2H),2.19−2.06(m,1H),2.04−1.84(m,2H),1.57−1.25(m,3H),1.06(s,3H),0.97−0.80(m,7H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.53,91.83,51.48,48.37,46.93,33.48,32.74,32.18,26.67,25.98,21.89.
SM[EI+](m/z)(%):214(M+,7),142(10),141(100),123(14),83(85),69(15),55(25),46(10),43(11),41(22).
1H−RMN(300MHz,CDCl3):δ(ppm)3.65(s,2H),2.19−2.06(m,1H),2.04−1.84(m,2H),1.57−1.25(m,3H),1.04(s,3H),0.97−0.80(m,7H).
13C−RMN(75MHz,CDCl3):δ(ppm)171.99,93.57,49.67,47.62,47.15,33.56,32.46,32.29,26.59,26.38,21.64.
SM[EI+](m/z)(%):214(M+,5),142(11),141(100),123(16),83(88),69(16),55(25),46(10),43(13),41(24),39(10).
896w、859w、798w、612w。
このようにして得られた8−ペンチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オンは、以下のスペクトル特徴を有する:
1H−RMN(300MHz,CDCl3):δ(ppm)3.67(s,2H),2.21−2.14(m,1H),2.06−1.90(m,2H),1.84−1.64(m,3H),1.40−1.11(m,11H),0.88−0.83(t,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.32,94.45,38.79,35.94,35.76,32.02,31.99,29.76,22.60,14.06.
SM[EI+](m/z)(%):242(M+,4),170(12),169(100),95(24),81(24),67(12),55(24),43(12),41(23).
1H−RMN(300MHz,CDCl3):δ(ppm)3.73(s,2H),2.21−2.14(m,1H),2.06−1.90(m,2H),1.84−1.64(m,3H),1.40−1.11(m,11H),0.88−0.83(t,J=7.2Hz,3H).
13C−RMN(75MHz,CDCl3):δ(ppm)172.32,91.61,39.58,35.97,35.49,32.31,31.75,29.53,26.58,22.62,14.27.
SM[e/m(%)]:242(M+,4),170(12),169(100),95(21),81(21),67(12),55(25),43(13),41(23).
IR(pure,cm−1):2922m,2853m,1769s,1443w,1209m,1184m,1133w,1041m,982m,901w,796w.
−8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン(化合物16025−37、実施例5、マッチB)
−8−エチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン(化合物16025−43、実施例2、マッチC)
−スピロ[4.5]デカン−8−オンのオキサチオラノン(化合物16025−56、実施例7、マッチD)
−8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン(化合物16025−37、実施例5、マッチB)
−8−エチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン(化合物16025−43、実施例2、マッチC)
−スピロ[4.5]デカン−8−オンのキサチオラノン(xathiolanone)(化合物16025−56、実施例7、マッチD)
一般に、香気の検出閾値による揮発性の比率は、分子の嗅覚的な力を考慮して、単位のない「香気値」を得ることを可能にすることが認められている。この値が大きいほど、問題の分子はより強力になる。この香気値を計算するために、揮発性および検出閾値を結果として決定する必要があります。
Claims (17)
- R5が飽和直鎖C1〜C5アルキル基を表す、請求項1に記載の化合物。
- R1、R2、R3、R4、R6およびR7が水素原子を表す、請求項1または2に記載の化合物。
- 炭素原子の総数が、10または11である、請求項1から3のいずれか一項に記載の化合物。
- 7,7−ジメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−エチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−エチル−3−メチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8,8−ジメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、3−メチル−8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、スピロ[4.5]デカン−8−オンのオキサチオラノン、7,7,9−トリメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オンおよび8−ペンチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オンの中から選択される、請求項1〜4のいずれか一項に記載の化合物。
- 7,7−ジメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−エチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−エチル−3−メチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8,8−ジメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、3−メチル−8−プロピル−1−オキサ−4−チアスピロ[4.5]デカン−2−オン、スピロ[4.5]デカン−8−オンのオキサチオラノン、7,7,9−トリメチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オンおよび8−ペンチル−1−オキサ−4−チアスピロ[4.5]デカン−2−オンの中から選択される少なくとも1種の化合物を含む、請求項6に記載の組成物。
- 式(I)の前記化合物が、前記組成物の総重量に対して0.000001〜50重量%、より具体的には0.000005〜20%に含まれる濃度で存在する、請求項6または7に記載の組成物。
- 少なくとも1種の式(I)の化合物および少なくとも1種の他の香気物質を含む香料組成物である、請求項6から8のいずれか一項に記載の組成物。
- 少なくとも1種の式(I)の化合物および少なくとも1種の他の芳香物質を含む芳香組成物である、請求項6から8のいずれか一項に記載の組成物。
- チオール酸がチオグリコール酸である、請求項11に記載の方法。
- チオール酸がチオ乳酸である、請求項11に記載の方法。
- 使用される酸がスルホン化パラトルエン酸である、請求項11から13のいずれか一項に記載の方法。
- 組成物または物品の物質の官能特性を付与、変更、または強化するための、立体異性体もしくは立体異性体の混合物、またはラセミ混合物の形態での、請求項1から5に記載のような一般式(I)の少なくとも1種の化合物の使用。
- 少なくとも1種の他の香気物質および/または少なくとも1種の溶媒および/または少なくとも1種の添加剤と組み合わせた、または個別の香味剤としての、式(I)の少なくとも1種の化合物の請求項15に記載の使用。
- 少なくとも1種の他の芳香物質および/または少なくとも1種の溶媒および/または少なくとも1種の添加剤と組み合わせた、または個別の芳香化合物としての、一般式(I)の少なくとも1種の化合物の請求項15に記載の使用。
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PCT/EP2019/051597 WO2019145347A1 (fr) | 2018-01-25 | 2019-01-23 | Nouveaux composés spirooxathiolanones, leur procédé de préparation ainsi que leur utilisation en parfumerie et aromatique |
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JP4590045B2 (ja) * | 1999-07-28 | 2010-12-01 | 長谷川香料株式会社 | 1,3−オキサチオラン−5−オン類およびそれを含有する香料組成物 |
RU2006119445A (ru) * | 2003-11-04 | 2007-12-27 | Фирмениш Са (Ch) | Ароматические ингридеенты для холодящих препаратов |
US8674143B2 (en) | 2008-10-15 | 2014-03-18 | Dsm Ip Assets, B.V. | Synthesis of green ketone intermediate |
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Patent Citations (2)
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JPS5632452A (en) * | 1979-08-27 | 1981-04-01 | Adeka Argus Chem Co Ltd | Novel thioketal compound |
JP2001316386A (ja) * | 2000-05-11 | 2001-11-13 | T Hasegawa Co Ltd | 環状置換基を有する1,3−オキサチオラン−5−オン類およびそれを含有する香料組成物 |
Non-Patent Citations (1)
Title |
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SYNTHETIC COMMUNICATIONS, vol. 33, no. 11, JPN6023000083, 2003, pages 1951 - 1961, ISSN: 0004959810 * |
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Publication number | Publication date |
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MA51663A (fr) | 2021-04-28 |
KR20200134216A (ko) | 2020-12-01 |
PH12020551105A1 (en) | 2021-05-31 |
FR3077074B1 (fr) | 2020-01-24 |
DK3743415T3 (da) | 2022-03-14 |
CA3089442A1 (fr) | 2019-08-01 |
MA51663B1 (fr) | 2022-03-31 |
ZA202004991B (en) | 2021-08-25 |
MX2020007778A (es) | 2021-01-15 |
EP3743415B1 (fr) | 2022-02-16 |
CL2020001925A1 (es) | 2021-02-12 |
PT3743415T (pt) | 2022-03-22 |
WO2019145347A1 (fr) | 2019-08-01 |
CN111989320A (zh) | 2020-11-24 |
US11359162B2 (en) | 2022-06-14 |
PL3743415T3 (pl) | 2022-05-30 |
RU2020126593A3 (ja) | 2022-02-25 |
JP7345503B2 (ja) | 2023-09-15 |
CN111989320B (zh) | 2023-07-11 |
US20210032563A1 (en) | 2021-02-04 |
RU2020126593A (ru) | 2022-02-25 |
FR3077074A1 (fr) | 2019-07-26 |
ES2909792T3 (es) | 2022-05-10 |
BR112020014882A2 (pt) | 2020-12-08 |
EP3743415A1 (fr) | 2020-12-02 |
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