Details
Purity 99% Min Sacubitril 149709-62-6 Spot Supply with Safe Transportation
- Molecular Formula:C24H29NO5
- Molecular Weight:411.498
- Boiling Point:656.9±55.0 °C(Predicted)
- PKA:4.72±0.10(Predicted)
- PSA:92.70000
- Density:1.151±0.06 g/cm3(Predicted)
- LogP:4.22590
149709-62-6 Relevant articles
Preparation method of sacubitril valsartan sodium
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Page/Page column 11-14, (2021/03/31)
The invention provides a preparation met...
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The preparation method comprises the fol...
AMMONIUM CARBOXYLATE COMPOUND, CRYSTALLINE FORM, AMORPHOUS FORM AND PREPARATION METHOD THEREOF
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Paragraph 170-171, (2020/03/01)
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149709-62-6 Process route
-
-
108-30-5
succinic acid anhydride
-
-
149690-12-0
(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoic acid ethyl ester hydrochloride
-
-
149709-62-6,149709-63-7,766480-48-2
α-ethyl (αR,γS)-γ-<(3-carboxy-1-oxopropyl)amino>-α-methyl<1,1'-biphenyl>-4-pentanoate
| Conditions | Yield |
|---|---|
|
With
N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 20 ℃;
for 0.5h;
|
88.3% |
|
With
triethylamine;
In
Isopropyl acetate;
at -5 - 30 ℃;
for 2h;
|
81.3% |
|
(2R,4S)-5-([1,1'-biphenyl]-4-yl)-4-amino-2-methylpentanoic acid ethyl ester hydrochloride;
With
triethylamine;
In
dichloromethane;
at 20 ℃;
for 0.166667h;
succinic acid anhydride;
In
dichloromethane;
at 0 ℃;
for 4h;
|
98.5 %Chromat. |
|
With
dmap; triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
for 3h;
|
165 g |
|
With
triethylamine;
In
Isopropyl acetate;
at 0 - 20 ℃;
for 2h;
|
|
|
With
triethylamine;
In
Isopropyl acetate;
at 20 ℃;
|
|
|
With
thionyl chloride;
for 8h;
|
98 % ee |
|
With
triethylamine;
In
ethyl acetate; toluene;
at 0 - 5 ℃;
for 4.33333h;
Reagent/catalyst;
Solvent;
Temperature;
|
|
|
With
N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 10 - 20 ℃;
|
36 g |
|
With
triethylamine;
In
dichloromethane;
at 25 - 30 ℃;
for 3h;
|
|
|
With
triethylamine;
In
water; ethyl acetate;
at 20 - 30 ℃;
for 2.5h;
|
|
|
With
pyridine;
at 60 - 70 ℃;
|
52.4 g |
|
With
N-ethyl-N,N-diisopropylamine;
In
Isopropyl acetate;
at 25 ℃;
for 4h;
Temperature;
Solvent;
|
|
|
With
N-ethyl-N,N-diisopropylamine;
In
Isopropyl acetate;
at 0 - 10 ℃;
for 6h;
|
-
-
108-30-5
succinic acid anhydride
-
-
752174-62-2,753421-85-1
(2R,4S)-4-amino-5-biphenyl-4-yl-2-methylpentanoic acid ethyl ester
-
-
149709-62-6,149709-63-7,766480-48-2
α-ethyl (αR,γS)-γ-<(3-carboxy-1-oxopropyl)amino>-α-methyl<1,1'-biphenyl>-4-pentanoate
| Conditions | Yield |
|---|---|
|
With
pyridine;
In
dichloromethane;
at 40 - 45 ℃;
for 10h;
|
77.9% |
|
succinic acid anhydride; (2R,4S)-4-amino-5-biphenyl-4-yl-2-methylpentanoic acid ethyl ester;
In
Isopropyl acetate;
at 20 ℃;
for 0.5h;
With
triethylamine;
In
Isopropyl acetate;
at -10 - 10 ℃;
|
|
|
With
pyridine;
In
dichloromethane;
|
|
|
With
triethylamine;
In
dichloromethane;
at 40 ℃;
for 1h;
Inert atmosphere;
Industrial scale;
|
13.9 g |
|
With
N-ethyl-N,N-diisopropylamine;
In
toluene;
at 5 - 10 ℃;
for 1h;
|
20 g |
149709-62-6 Upstream products
-
149709-64-8
α-ethyl (αR,γS)-γ-<<3-(1,1-dimethylethoxy)-1-oxopropyl>amino>-α-methyl<1,1'-biphenyl>-4-pentanoate
-
128779-47-5
(2R)-3-(biphenyl-4-yl)-2-[(tert-butoxycarbonyl)amino]propanoic acid
-
76757-90-9
N-(tert-butoxycarbonyl)-D-tyrosine methyl ester
-
753421-85-1
ethyl (γS)-γ-amino-α-methyl<1,1'-biphenyl>-4-pentanoate
149709-62-6 Downstream products
-
149690-05-1
α-ethyl (αR,γS)-γ-<(3-carboxy-1-oxopropyl)amino>-α-methyl<1,1'-biphenyl>-4-pentanoate monosodium salt
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