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Chemical Structure| 874801-60-2 Chemical Structure| 874801-60-2

Structure of 874801-60-2

Chemical Structure| 874801-60-2

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Product Details of [ 874801-60-2 ]

CAS No. :874801-60-2
Formula : C14H17N3O3S
M.W : 307.37
SMILES Code : O=C(N(C1)CCC2=C1SC(N=CN3)=C2C3=O)OC(C)(C)C
MDL No. :MFCD05664943

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Application In Synthesis of [ 874801-60-2 ]

* 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 [ 874801-60-2 ]

[ 874801-60-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3473-63-0 ]
  • [ 193537-14-3 ]
  • [ 874801-60-2 ]
YieldReaction ConditionsOperation in experiment
90% In N,N-dimethyl-formamide; at 100℃; for 16.0h; 4-Oxo-3,5,6,8-tetrahydro-4H-9-thia-1,3,7-triaza-fluorene-7-carboxylic acid tert-butyl ester (step b). A mixture of 2-amino-4,7-dihydro-5H-thieno[2,3-c]pyridine-3,6-dicarboxylic acid 6-tert-butyl ester 3-ethyl ester (18.5 g) and formamidine acetate (8.85 g) in DMF (100 mL) were heated at 100 C. for 16 h. The reaction mixture was cooled and concentrated. The residues was partitioned between water and ethyl acetate. The organic layer was washed with water 3 times and concentrated to give the title compound (15.8 g, 90%). 1H NMR (400 MHz, CDCl3): delta 7.88 (s, 1H), 4.56-4.62 (brs, 2H), 3.62-3.70 (brs, 2H), 3.02-3.08 (brs, 2H), 1.42 (s, 9H). LC-MS (ESI) m/z 308.1 (M+H).
90.6% In N,N-dimethyl-formamide; at 100℃; To a <strong>[193537-14-3]2-Amino-4,7-dihydro-5H-thieno[2,3-c]pyridine-3,6-dicarboxylic acid 6-tert-butyl ester 3-ethyl ester</strong> (5.0 g, 15 mmol) in DMF (50 mL) solution was added formamidine acetate (2.39 g, 23 mmol, 1.5 equiv). The mixture was heated at 100 C. in an oil bath for overnight. The reaction mixture was cooled to rt and then concentrated in vacuo. Ethyl acetate (50 mL) was added to the reaction solid mixture and stirred at rt for 2 h. The mixture was then filtered, rinsed with ethyl acetate (25 mL). The solid was placed in a vacuum oven and dried for overnight to yield a white solid (4.17 g, 90.6%). 1H NMR (CD3OD-d4) delta 8.05 (s, 1H), 4.57 (s, 2H), 3.61 (t, 2H), 2.92 (t, 2H), 1.42 (s, 9H); LCMS RT=2.78 min, [M+H]+=308.0.
88% In N,N-dimethyl-formamide; at 100℃; To a solution of 6-tert-butyl 3-ethyl 2-amino-4,7-dihydrothieno[2,3-c]pyridine-3,6(5H)-dicarboxy- late from Example 9A (1.23 kg, 3.77 mol) in DMF (10.3 L) was added formamidine acetate (588 g, 5.65 mol). The mixture was heated to 1000C overnight. The solvent was removed in vacuo. The residue was stirred with ethyl acetate (3 L) for 2 h. The precipitate was collected by suction filtration and rinsed with ethyl acetate. The solid was dried to yield 1.02 kg (88%) of the title compound.1H-NMR (400 MHz, DMSOd6): delta = 1.43 (s, 9H), 2.91-2.96 (m, 2H), 3.62 (t, 2H), 4.58 (s, 2H), 8.05 (s, IH), 12.38 (br. s, IH).LC/MS (method 4): R, = 2.03 min; MS (ESIpos): m/z = 308 [M+H]+.
In N,N-dimethyl-formamide; at 120℃; for 16.0h; The N-(tert-Butoxycarbonyl)-4-piperidone, NCCH2CO2Et and Et3N was mixed at roomtemperature then stirring for 16 h, and then heated to 120 C for 16 h in DMF with the formamidineacetate. Then, the intermediate was reacted with POCl3 and DIPEA in toluene to obtain thecompound 7 (yield 89%).

  • 2
  • [ 463-52-5 ]
  • [ 193537-14-3 ]
  • [ 874801-60-2 ]
YieldReaction ConditionsOperation in experiment
90% In N,N-dimethyl-formamide; at 100℃; for 16.0h; General procedure: A mixture of (2) (4.50 g, 20.0 mmol) andformamidine acetate (3.12 g, 30.0 mmol) was sterred in DMF for 12 hat 100 C. The reaction mixture was cooled, water was added, and theprecipitate formed was collected by filtration, and washed thoroughlywith water to give 3, Yield, 91%.
 

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