Technology Process of 1,3,11,16-Nonadecatetraen-6-ol,
8,14-bis[(4-methoxyphenyl)methoxy]-5,7,13,15-tetramethyl-19-[(2S,3R,
4S,5R,6R)-tetrahydro-6-methoxy-4-(methoxymethoxy)-3,5-dimethyl-2H-
pyran-2-yl]-, carbamate, (3Z,5S,6S,7S,8R,11Z,13S,14R,15S,16Z)-
There total 38 articles about 1,3,11,16-Nonadecatetraen-6-ol,
8,14-bis[(4-methoxyphenyl)methoxy]-5,7,13,15-tetramethyl-19-[(2S,3R,
4S,5R,6R)-tetrahydro-6-methoxy-4-(methoxymethoxy)-3,5-dimethyl-2H-
pyran-2-yl]-, carbamate, (3Z,5S,6S,7S,8R,11Z,13S,14R,15S,16Z)- which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
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-
565229-72-3
carbamic acid, (1S,2S,3R,6Z,8S,9S,10S,11Z)-3,9-bis(4-methoxybenzyloxy)-14-[(2S,3S,4S,5R,6R)-6-methoxy-4-methoxymethoxy-3,5-dimethyltetrahydropyran-2-yl]-2,8,10-trimethyl-1-[(1S,2Z)-1-methylpenta-2,4-dienyl]tetradeca-6,11-dienyl ester
- Guidance literature:
-
With
water; potassium carbonate;
In
methanol;
at 20 ℃;
for 3h;
-
-
(3Z,11Z,16Z)-(5S,6S,7R,8R,13S,14R,15S)-8,14-Bis-(4-methoxy-benzyloxy)-19-((2S,3R,4S,5R,6R)-6-methoxy-4-methoxymethoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-5,7,13,15-tetramethyl-nonadeca-1,3,11,16-tetraen-6-ol
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-
565229-72-3
carbamic acid, (1S,2S,3R,6Z,8S,9S,10S,11Z)-3,9-bis(4-methoxybenzyloxy)-14-[(2S,3S,4S,5R,6R)-6-methoxy-4-methoxymethoxy-3,5-dimethyltetrahydropyran-2-yl]-2,8,10-trimethyl-1-[(1S,2Z)-1-methylpenta-2,4-dienyl]tetradeca-6,11-dienyl ester
- Guidance literature:
-
(3Z,11Z,16Z)-(5S,6S,7R,8R,13S,14R,15S)-8,14-Bis-(4-methoxy-benzyloxy)-19-((2S,3R,4S,5R,6R)-6-methoxy-4-methoxymethoxy-3,5-dimethyl-tetrahydro-pyran-2-yl)-5,7,13,15-tetramethyl-nonadeca-1,3,11,16-tetraen-6-ol; Trichloroacetyl isocyanate;
In
dichloromethane;
at 20 ℃;
for 0.5h;
With
potassium carbonate;
In
methanol;
at 20 ℃;
for 3h;
DOI:10.1021/jm0204136
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-
565229-72-3
carbamic acid, (1S,2S,3R,6Z,8S,9S,10S,11Z)-3,9-bis(4-methoxybenzyloxy)-14-[(2S,3S,4S,5R,6R)-6-methoxy-4-methoxymethoxy-3,5-dimethyltetrahydropyran-2-yl]-2,8,10-trimethyl-1-[(1S,2Z)-1-methylpenta-2,4-dienyl]tetradeca-6,11-dienyl ester
- Guidance literature:
-
Multi-step reaction with 13 steps
1.1: Bu2BOTf; N,N-diisopropylethylamine / CH2Cl2 / 0.5 h / 0 °C
1.2: CH2Cl2 / 2.17 h / -78 - 0 °C
1.3: 2.29 g / aq. H2O2; phosphate buffer / CH2Cl2; methanol / 1 h / pH 7.0
2.1: 92 percent / N,N-diisopropylethylamine / CH2Cl2 / Heating
3.1: 83 percent / HF*pyridine; pyridine / methanol / 48 h / 20 °C
4.1: diisobutylaluminum hydride / tetrahydrofuran; CH2Cl2 / 1 h / -78 °C
5.1: pyridinium p-toluenesulfonate / 15 h / 20 °C
6.1: H2 / Pd/C / ethyl acetate / 3 h / 20 °C / atmospheric pressure
7.1: 274 mg / Dess-Martin periodinane / CH2Cl2 / 20 °C
8.1: NaHMDS / tetrahydrofuran / 0.33 h / 20 °C
8.2: 67 percent / tetrahydrofuran / 4.33 h / -78 - 20 °C
9.1: diisobutylaluminum hydride / hexane; CH2Cl2 / 2 h / 0 °C
10.1: 267 mg / Dess-Martin periodinane / CH2Cl2
11.1: 52 percent / NaHMDS / tetrahydrofuran / 4.33 h / -78 - 20 °C
12.1: tetrabutylammonium fluoride / tetrahydrofuran / 48 h / 20 °C
13.1: CH2Cl2 / 0.5 h / 20 °C
13.2: 72 percent / K2CO3 / methanol / 3 h / 20 °C
With
pyridine; di-n-butylboryl trifluoromethanesulfonate; tetrabutyl ammonium fluoride; hydrogen; sodium hexamethyldisilazane; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; Dess-Martin periodane; pyridine hydrogenfluoride; N-ethyl-N,N-diisopropylamine;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; hexane; dichloromethane; ethyl acetate;
7.1: Dess-Martin oxidation / 8.2: Wittig olefination / 10.1: Dess-Martin oxidation / 11.1: Wittig olefination;
DOI:10.1021/jm0204136