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Home > Products >  Dolutegravir intermediate

Dolutegravir intermediate CAS NO.1335210-35-9

  • Min.Order: 1 Kilogram
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  • Product Details

Keywords

  • (4R,12aS)-N-(2,4-Difluorobenzyl)-7-Methoxy-4-Methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-[1,3]oxazino[3,2-d]pyrido[1,2-a]pyrazine-9-carboxaMide
  • Dolutegravir
  • 1335210-35-9

Quick Details

  • ProName: (4R,12aS)-N-(2,4-Difluorobenzyl)-7-Met...
  • CasNo: 1335210-35-9
  • Molecular Formula: C21H21F2N3O5
  • Appearance: White crystallization
  • Application: treating pulmonary embolism and preven...
  • DeliveryTime: in two weeks
  • PackAge: 25kg/drum
  • Port: SHANGHAI BEIJING
  • ProductionCapacity: 10 Metric Ton/Day
  • Purity: 99.9% by HPLC
  • Transportation: AIR SEA TRAIN
  • LimitNum: 1 Kilogram
  • Moisture Content: ≤0.5%

Superiority

We are very compeitive on Dolutegravir .Our mfr is Chinese GMP certified for this item with DMF document.

Product Name: O-Methyl Dolutegravir
CAS: 1335210-35-9
MF: C21H21F2N3O5
MW: 433.41
EINECS:  
Product Categories: CMLLYL
Mol File: 1335210-35-9.mol
O-Methyl Dolutegravir Structure
 
O-Methyl Dolutegravir Chemical Properties
Boiling point  684.3±55.0 °C(Predicted)
density  1.45±0.1 g/cm3(Predicted)
storage temp.  Sealed in dry,Room Temperature
pka 10.70±0.40(Predicted)
 
Safety Information
HS Code  38220090

Details

Description Dolutegravir intermediate is a new synthetic intermediate of Dolutegravir. Dolutegravir is an integrase inhibitor used to treat human immunodeficiency virus (HIV)-1 infection.
Uses (4R,12AS)-N-(2,4-Difluorobenzyl)-7-methoxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1'',2'':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide is an intermediate in the preparation of dolutegravir, an integrase inhibitor for HIV-1 infection therapy.
Synthesis (3S,11aR)-3-methyl-6-(methyloxy)-5,7-dioxo-2,3,5,7,11,11a- hexahydro[1,3]oxazolo [3,2-a]pyrido[1,2-d]pyrazine-8-carboxylic acid (100 gm) and carbonyl dimidazole (78.89 gm) was suspended in acetonitrile (1000 mL). The mixture was heated to 75°C and stirred for 1 hour. The resulting solution was cooled to a temperature of 20°C and treated with 2,4- difluorobenzyl amine solution (55.2 gm was dissolved in 200 mL of acetonitrile). The reaction mixture was maintained for 2 hours, concentrated, and the compound was extracted with ethyl acetate (1000 mL). Isopropyl alcohol (500 mL) was added at 40°C, stirred the reaction mass for 30 minutes at a temperature of 50°C, and cooled the reaction mass to 25°C. The reaction mixture was maintained for 8 hours at the same temperature. The product O-Methyl Dolutegravir was collected by filtration and dried under vacuum (85 gm).
O-Methyl Dolutegravir
 
O-Methyl Dolutegravir Preparation Products And Raw materials
Raw materials (4R,12aS)-7-Methoxy-4-Methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-[1,3]oxazino[3,2-d]pyrido[1,2-a]pyrazine-9-carboxylic acid-->2,4-Difluorobenzylamine
Preparation Products Dolutegravir sodium

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