L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester
- Product Name
- L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester
- CAS No.
- 1256490-52-4
- Chemical Name
- L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester
- Synonyms
- Sofosbuvir-003-S;2-naphthalen-7-ylethanamine;Octanedioicacid,3,11-dioxo-,dimethylester;(S)-Sofosbuvir Pentafluorophenoxy Analogue;N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-...;Isopropyl ((perfluorophenoxy)(phenoxy)phosphoryl)-L-alaninate;(2S)-Isopropyl 2-((perfluorophenoxy)(phenoxy)phosphorylamino...;N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester;Isopropyl (2S)-2-[[(Perfluorophenoxy)(phenoxy)phosphoryl]amino]propanoate;propan-2-yl (2S)-2-{[pentafluorophenoxy(phenoxy)phosphoryl]amino}propanoate
- CBNumber
- CB42704706
- Molecular Formula
- C18H17F5NO5P
- Formula Weight
- 453.3
- MOL File
- 1256490-52-4.mol
L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester Property
- Boiling point:
- 442.6±55.0 °C(Predicted)
- Density
- 1.405±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- -3.81±0.70(Predicted)
N-Bromosuccinimide Price
- Product number
- 122537
- Product name
- Isopropyl(2S)-2-[[(2,3,4,5,6-pentafluorophenoxy)-phenoxy-phosphoryl]amino]propanoate
- Purity
- 97.0%
- Packaging
- 1g
- Price
- $594
- Updated
- 2021/12/16
- Product number
- 1256490524
- Product name
- (2S)-Isopropyl2-(((perfluorophenoxy)(phenoxy)phosphoryl)amino)propanoate
- Packaging
- 25g
- Price
- $597.4
- Updated
- 2021/12/16
- Product number
- BD300401
- Product name
- (2S)-Isopropyl2-(((perfluorophenoxy)(phenoxy)phosphoryl)amino)propanoate
- Purity
- 95+%
- Packaging
- 100g
- Price
- $1016
- Updated
- 2021/12/16
- Product number
- A621578
- Product name
- (2S)-Isopropyl2-(((perfluorophenoxy)(phenoxy)phosphoryl)amino)propanoate
- Purity
- 95%
- Packaging
- 100g
- Price
- $1043
- Updated
- 2021/12/16
- Product number
- A621578
- Product name
- (2S)-Isopropyl2-(((perfluorophenoxy)(phenoxy)phosphoryl)amino)propanoate
- Purity
- 95%
- Packaging
- 1g
- Price
- $31
- Updated
- 2021/12/16
L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester Chemical Properties,Usage,Production
Synthesis
261909-49-3
771-61-9
1256490-52-4
GENERAL STEPS: In a reaction flask equipped with a mechanical stirrer, a reflux condenser tube, a thermometer, and under nitrogen protection, a solution of (L)-alanine isopropyl ester hydrochloride (Q) (2.8 g, 16.8 mmol) prepared in Example 1 was added with methylene chloride (21 mL). The mixture was stirred at room temperature until a homogeneous suspension was formed. Subsequently, the mixture was cooled to -65°C to -55°C using a dry ice-acetone bath and triethylamine (3.9 g, 38.8 mmol) was added slowly, ensuring that the temperature was maintained below -50°C. The mixture was then cooled to -65°C to -55°C using a dry ice-acetone bath. After addition, cooling was continued to -65°C to -55°C and a solution of dichloromethane (11 mL) of phenyl dichlorophosphate (3.3 g, 15.6 mmol) was added dropwise, controlling the temperature to below -50°C. The reaction mixture was stirred at -65°C to -55°C until the reaction was complete (about 1 h). In another reaction flask equipped with the same apparatus, pentafluorophenol (2.4 g, 13.0 mmol) and dichloromethane (28 mL) were added. The mixture was cooled to 0°C to 5°C and triethylamine (1.6 g, 15.8 mmol) was added slowly, keeping the temperature below 10°C. After the addition, the temperature was raised to 20°C to 25°C and maintained for 1 h. It was then added to the previously prepared mixture, which had to be cooled down to -15°C to -10°C and ensuring that the internal temperature did not exceed 5°C. After the addition, the reaction mixture was After addition, the reaction mixture is warmed to 0°C to 5°C and maintained until the reaction is complete (about 1 hour). Water (8.7 mL) was added to the reaction system and the temperature was controlled to be below 10°C. The reaction was then warmed to 20°C to 25°C, partitioned, and the organic phase was washed with water and concentrated to dryness under reduced pressure. The residual solvent was removed by azeotropic isopropyl acetate to give 9.0 g of residue (quantitative yield) with diastereoisomer ratio Sp:flp = 50:50.
References
[1] Patent: WO2016/151542, 2016, A1. Location in patent: Page/Page column 23; 24
[2] Patent: WO2014/62596, 2014, A1. Location in patent: Page/Page column 60
[3] Patent: US2014/206640, 2014, A1. Location in patent: Paragraph 0286; 0287
[4] Patent: CN106543253, 2017, A. Location in patent: Paragraph 0086-0089
[5] Patent: WO2018/48937, 2018, A1. Location in patent: Page/Page column 220; 221
L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester Preparation Products And Raw materials
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View Lastest Price from L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester manufacturers
- Product
- L-Alanine, N-[(2,3,4,5,6-pentafluorophenoxy)phenoxyphosphinyl]-, 1-Methylethyl ester 1256490-52-4
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 200kgs
- Release date
- 2020-02-18