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Chemical Structure| 141120-33-4 Chemical Structure| 141120-33-4

Structure of 141120-33-4

Chemical Structure| 141120-33-4

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Product Details of [ 141120-33-4 ]

CAS No. :141120-33-4
Formula : C9H16O5S
M.W : 236.29
SMILES Code : CS(=O)(OC(CC1)CCC21OCCO2)=O
MDL No. :MFCD09953114

Safety of [ 141120-33-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 141120-33-4 ]

* 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.

  • Downstream synthetic route of [ 141120-33-4 ]

[ 141120-33-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 612501-52-7 ]
  • [ 141120-33-4 ]
  • [ 1046137-43-2 ]
YieldReaction ConditionsOperation in experiment
47% With potassium carbonate; In N,N-dimethyl-formamide; at 50 - 80℃; At 50 C. 12.5 g potassium carbonate and 16 g 8-methanesulphonyloxy-1,4-dioxa-spiro[4,5]decane (cf for example Journal of Medicinal Chemistry (1992), 35(12), 2243-7) are added to 18.1 g <strong>[612501-52-7]4-[(3-chloro-2-fluoro-phenyl)amino]-6-hydroxy-7-methoxy-quinazoline</strong> (cf for example Bioorganic & Medicinal Chemistry Letters (2006), 16(18), 4908-4912) in 125 ml dimethylformamide and the mixture is stirred for 18 hours at 80 C. Another 4.7 g potassium carbonate and 4.0 g of 8-methanesulphonyloxy-1,4-dioxa-spiro[4,5]decane are added and the mixture is stirred for another 7 hours at 80 C. The reaction mixture is cooled, diluted with water and ethyl acetate and the precipitate formed is suction filtered and dried.Yield: 12.2 g (47% of theory)Mass spectrum (ESI+): m/z=460, 462 [M+H]+
47% With potassium carbonate; In N,N-dimethyl-formamide; at 50 - 80℃; for 25h; 12.5 g potassium carbonate and 16 g 8-methanesulphonyloxy-1,4-dioxa-spiro[4.5]decan (cf. for example Journal of Medicinal Chemistry (1992), 35(12), 2243-7) in 125 ml dimethylformamide are added at 50 C. to 18.1 g <strong>[612501-52-7]4-[(3-chloro-2-fluoro-phenyl)amino]-6-hydroxy-7-methoxy-quinazoline</strong> (cf. for example Bioorganic & Medicinal Chemistry Letters (2006), 16(18), 4908-4912) and the mixture is stirred for 18 hours at 80 C. Another 4.7 g potassium carbonate and 4.0 g 8-methanesulphonyloxy-1,4-dioxa-spiro[4.5]decan are added and the mixture is stirred for a further 7 hours at 80 C. The reaction mixture is cooled, diluted with water and ethyl acetate and the precipitate formed is suction filtered and dried. Yield: 12.2 g (47% of theory) Mass spectrum (ESI+): m/z=460, 462[M+H]+
 

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