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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
DLinDMA is a key lipid component of stable nucleic acid lipid particles as a benchmark.
Synonyms: 1,2-Dilinoleyloxy-N,N-dimethyl-3-aminopropane
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| CAS No. : | 871258-12-7 |
| Formula : | C41H77NO2 |
| M.W : | 616.06 |
| SMILES Code : | CN(C)CC(COCCCCCCCC/C=C\C/C=C\CCCCC)OCCCCCCCC/C=C\C/C=C\CCCCC |
| Synonyms : |
1,2-Dilinoleyloxy-N,N-dimethyl-3-aminopropane
|
| MDL No. : | MFCD31715447 |
| InChI Key : | NFQBIAXADRDUGK-KWXKLSQISA-N |
| Pubchem ID : | 11570822 |
| GHS Pictogram: |
|
| Signal Word: | Warning |
| Hazard Statements: | H302-H315-H319-H335 |
| Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 60% | Synthesis of 1, 2-DiLinoleyloxy-N,N-dimethylaminopropane (DLinDMA) and 1,2-Dilinolenyloxy-N,N-dimethylaminopropane (DLenDMA) (0249) 3-(Dimethylamino)-1,2-propanediol (714 mg, 6 mmol) and 95% sodium hydride (NaH, 1.26 g, 50 mmol) are stirred in benzene (30 mL) under nitrogen for 30 minutes. Linoleyl mesylate (5.0 g, 15 mmol) is added and the reaction refluxed under nitrogen for 3 hours. The reaction mixture is then cooled in an ice bath while quenching via the slow addition of ethanol. Following dilution with a further 150 mL of benzene, the mixture is washed with distilled water (2×150 mL) and brine (150 mL). The organic phase is dried over magnesium sulphate and evaporated to give the crude product. (0250) The crude product is purified on a silica gel (Kiesel Gel 60) column eluted with 0-5% methanol in chloroform. Column fractions are analyzed by thin layer chromatography (TLC) (silica gel, chloroform/methanol 9:1 v/v, visualized with molybdate dip) and fractions containing purified product (Rf=0.5) are pooled and concentrated. (0251) Decolorization and further purification of DLinDMA is effected with a second column, this time eluting with 20-50% ethyl acetate in hexane. Column fractions are analyzed by TLC (silica gel, ethyl acetate/hexane 1:1 v/v, visualized with molybdate) and fractions containing pure product (Rf=0.4) are pooled and concentrated. The procedure described herein typically yields 2.2 g (60%) of pure product. | |
| EXAMPLE 2SYNTHESIS OF 1 ,2-DILINOLEYLOXY-N1N-DIMETHYL-S-AMINOPROPANE (DLINDMA) DLinDMA was synthesized as described below.1 ,2-Dilinoleyloxy-3-dimethylaminopropane (DLinDMA)To a suspension of NaH (95%, 5.2 g, 0.206 mol) in 120 mL of anhydrous benzene was added dropwise N,N-dimethyl-3-aminopropane-1 ,2- diol (2.8 g, 0.0235 mol) in 40 mL of anhydrous benzene under argon. Upon addition, the resulting mixture was stirred at room temperature for 15 min. Linoleyl methane sulfonate (99%, 20 g, 0.058 mol) in 75 mL of anhydrous benzene was added dropwise at room temperature under argon to the above mixture. After stirred at room temperature for 30 min., the mixture was refluxed overnight under argon. Upon cooling, the resulting suspension was treated dropwise with 250 ml_ of 1 :1 (V:V) ethanol-benzene solution. The organic phase was washed with water (150 ml_), brine (2 x 200 ml_), and dried over anhydrous sodium sulfate. Solvent was evaporated in vacuo to afford 17.9 g of light oil as a crude product. 10.4 g of pure DLinDMA were obtained upon purification of the crude product by column chromatography twice on silica gel using 0-5% methanol gradient in methylene chloride. 1 H NMR (400 MHz, CDCI3) delta: 5.35 (8H, m, CH=CH), 3.5 (7H, m, OCH), 2.75 (4H, t, 2 x CH2), 2.42 (2H, m, NCH2), 2.28 (6H, s, 2 x NCH3), 2.05 (8H, q, vinyl CH2), 1.56 (4H, m, 2 x CH2), 1.28 (32H, m, 16 x CH2), 0.88 (6H, t, 2 x CH3) ppm. | ||
| To a suspension of NaH (95%, 5.2 g, 0.206 mol) in 120 mL of anhydrous benzene was added dropwise N,N-dimethyl-3-aminopropane-1,2-diol (2.8 g, 0.0235 mol) in 40 mL of anhydrous benzene under argon. Upon addition, the resulting mixture was stirred at room temperature for 15 min. Linoleyl methane sulfonate (99%, 20 g, 0.058 mol) in 75 mL of anhydrous benzene was added dropwise at room temperature under argon to the above mixture. After stirred at room temperature for 30 min., the mixture was refluxed overnight under argon. Upon cooling, the resulting suspension was treated dropwise with 250 mL of 1:1 (V:V) ethanol-benzene solution. The organic phase was washed with water (150 mL), brine (2×200 mL), and dried over anhydrous sodium sulfate. Solvent was evaporated in vacuo to afford 17.9 g of light oil as a crude product. 10.4 g of pure DLinDMA were obtained upon purification of the crude product by column chromatography twice on silica gel using 0-5% methanol gradient in methylene chloride. 1H NMR (400 MHz, CDCl3) delta: 5.35 (8H, m, CHCH), 3.5 (7H, m, OCH), 2.75 (4H, t, 2×CH2), 2.42 (2H, m, NCH2), 2.28 (6H, s, 2×NCH3), 2.05 (8H, q, vinyl CH2), 1.56 (4H, m, 2×CH2), 1.28 (32H, m, 16×CH2), 0.88 (6H, t, 2×CH3) ppm |
| 10.4 g | [0211] To a suspension of NaH (95%, 5.2 g, 0.206 mol) in 120 mL of anhydrous benzene was added dropwise N,Ndimethyl-3-aminopropane-1,2-diol (2.8 g, 0.0235 mol) in 40 mL of anhydrous benzene under argon. Upon addition, theresulting mixture was stirred at room temperature for 15 min. Linoleyl methane sulfonate (99%, 20 g, 0.058 mol) in 75mL of anhydrous benzene was added dropwise at room temperature under argon to the above mixture. After stirred atroom temperature for 30 min., the mixture was refluxed overnight under argon. Upon cooling, the resulting suspensionwas treated dropwise with 250 mL of 1:1 (V:V) ethanol-benzene solution. The organic phase was washed with water(150 mL), brine (2 x 200 mL), and dried over anhydrous sodium sulfate. Solvent was evaporated in vacuo to afford 17.9g of light oil as a crude product. 10.4 g of pure DLinDMA were obtained upon purification of the crude product by columnchromatography twice on silica gel using 0-5% methanol gradient in methylene chloride. 1 H NMR (400 MHz, CDCl3)delta: 5.35 (8H, m, CH=CH), 3.5 (7H, m, OCH), 2.75 (4H, t, 2 x CH2), 2.42 (2H, m, NCH2), 2.28 (6H, s, 2 x NCH3), 2.05 (8H,q, vinyl CH2), 1.56 (4H, m, 2 x CH2), 1.28 (32H, m, 16 x CH2), 0.88 (6H, t, 2 x CH3) ppm. |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 2.73 g | 2) 500ml four-necked flask was added sodium hydride 1.5g, tetrahydrofuran 50ml, stirring evenly, argon protection. 3 - (dimethylamino) -1,2 - propanediol lg by constant pressure dropping funnel dropping, lOmins drop finished,Dropping p-toluenesulfonic acid linoleic oil 9g, 0.5h drop finished, heated to 66 degrees, micro-reflux reaction 24h, the color is light yellow, after cooling, Buchner funnel suction filter, petroleum ether extract filtrate, combined washed organic phase , Dried over anhydrous magnesium sulfate, spin off the solution, the red oil l0g. Silica gel column chromatography, eluent Dichloromethane: Methanol 10: 1 Separation 2.73 g of a pale yellow oil |
Tags: DLinDMA | 1,2-Dilinoleyloxy-N,N-dimethyl-3-aminopropane | Cationic Lipids | Drug Delivery | 871258-12-7
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