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Chemical Structure| 1446091-46-8 Chemical Structure| 1446091-46-8

Structure of 1446091-46-8

Chemical Structure| 1446091-46-8

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Product Details of [ 1446091-46-8 ]

CAS No. :1446091-46-8
Formula : C18H14N2O5
M.W : 338.31
SMILES Code : O=C([C@@H]1[C@@]2([H])OC3=CC=C(OC4=CC=NC5=C4CCC(N5)=O)C=C3[C@]21[H])O

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Application In Synthesis of [ 1446091-46-8 ]

* 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 [ 1446091-46-8 ]

[ 1446091-46-8 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 1237535-78-2 ]
  • [ 1446091-43-5 ]
  • [ 1446091-45-7 ]
  • [ 1446091-46-8 ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In N,N-dimethyl-formamide; at 40 - 120℃; for 3h;Large scale; To a solution of Intermediate 6 (14 kg) and 5-fluoro-3, 4-dihydro-1, 8-naphthyridin-2 (1H) -one (SM2, 11.2kg) in DMF (66kg) was added Cs2CO3(26kg) at 4060, and the mixture was warmed to 110120 and stirred for 3hrs at 110120. The reaction pH was adjusted to 6 with acetic acid (12.0 kg) at 2535. Water (520kg) was added and the mixture was stirred for 12hrs. After filtration, the solid was slurried with EA (78kg) to get a wet product (the purity: (Intermediate 7 + Intermediate 8) : 98) . An aqueous sodium hydroxide solution (125kg, 2M) was added to a stirred solution of the wet product in THF (240kg) and stirred for 23hrs at 2030 (IPC: INT-7/INT-8: 0.9) . The mixture was adjusted to pH 45 with 4N HCl (37kg) at 2030 and then stirred for 0.51h. The mixture was concentrated at below 50 and a solid precipitated out of the solution. After filtration, the wet product was re-slurried in THF at 3545 for 12hrs, and then filtered. The resultant wet product was dried for 40hrs at 4565 to give the title compound Intermediate 8 (18.95kg: chemical purity 99, chiral purity 100) .1H NMR (400 MHz, DMSO-d6) delta 12.59 (s, 1H) , 10.43 (s, 1H) , 7.92 (d, J 5.8 Hz, 1H) , 7.29 (d, J 2.4 Hz, 1H) , 6.97 (d, J 8.8 Hz, 1H) , 6.93 (dd, J 8.8, 2.4 Hz, 1H) , 6.21 (d, J 5.8 Hz, 1H) , 5.21 (dd, J 5.4, 1.0 Hz, 1H) , 3.27 -3.25 (m, 1H) , 2.89 (t, J 7.8 Hz, 2H) , 2.51 (d, J 8.8 Hz, 2H) , 1.19 (dd, J 3.0, 1.0 Hz, 1H) ppm. MS: M/e 339 (M+1)+.
  • 3
  • [ 1237535-78-2 ]
  • [ 1446091-43-5 ]
  • [ 1446091-46-8 ]
YieldReaction ConditionsOperation in experiment
18.95 kg To a solution of Intermediate 6 (14 kg) and 5-fluoro-3, 4-dihydro-1, 8-naphthyridin-2 (1H) -one (SM2, 11.2kg) in DMF (66kg) was added Cs2CO3(26kg) at 4060, and the mixture was warmed to 110120 and stirred for 3hrs at 110120. The reaction pH was adjusted to 6 with acetic acid (12.0 kg) at 2535. Water (520kg) was added and the mixture was stirred for 12hrs. After filtration, the solid was slurried with EA (78kg) to get a wet product (the purity: (Intermediate 7 + Intermediate 8) : 98) . An aqueous sodium hydroxide solution (125kg, 2M) was added to a stirred solution of the wet product in THF (240kg) and stirred for 23hrs at 2030 (IPC: INT-7/INT-8: 0.9) . The mixture was adjusted to pH 45 with 4N HCl (37kg) at 2030 and then stirred for 0.51h. The mixture was concentrated at below 50 and a solid precipitated out of the solution. After filtration, the wet product was re-slurried in THF at 3545 for 12hrs, and then filtered. The resultant wet product was dried for 40hrs at 4565 to give the title compound Intermediate 8 (18.95kg: chemical purity 99, chiral purity 100) .1H NMR (400 MHz, DMSO-d6) delta 12.59 (s, 1H) , 10.43 (s, 1H) , 7.92 (d, J 5.8 Hz, 1H) , 7.29 (d, J 2.4 Hz, 1H) , 6.97 (d, J 8.8 Hz, 1H) , 6.93 (dd, J 8.8, 2.4 Hz, 1H) , 6.21 (d, J 5.8 Hz, 1H) , 5.21 (dd, J 5.4, 1.0 Hz, 1H) , 3.27 -3.25 (m, 1H) , 2.89 (t, J 7.8 Hz, 2H) , 2.51 (d, J 8.8 Hz, 2H) , 1.19 (dd, J 3.0, 1.0 Hz, 1H) ppm. MS: M/e 339 (M+1)+.
18.95 kg To a solution of Intermediate 6 (14 kg) and 5-fluoro-3,4-dihydro-l,8-naphthyridin-2(lH)- one (SM2, 11.2kg) in DMF (66kg) was added Cs2C03 (26kg) at 40~60C, and the mixture was warmed to 110~120C and stirred for 3 hours at 110~120C. The reaction pH was adjusted to 6 with acetic acid (12.0 kg) at 25~35C. Water (520kg) was added and the mixture was stirred for 1-2 hours. After filtration, the solid was slurried with EA (78kg) to get a wet product (the purity: (Intermediate 7 + Intermediate 8) %: 98%). An aqueous sodium hydroxide solution (125kg, 2M) was added to a stirred solution of the wet product in THF (240kg) and stirred for 2-3 hours at 20~30C (IPC: INT-7/INT-8: 0.9%). The mixture was adjusted to pH 4-5 with 4N HC1 (37kg) at 20~30C and then stirred for 0.5~lh. The mixture was concentrated at below 50C and a solid precipitated out of the solution. After filtration, the wet product was re-slurried in THF at 35~45C for 1-2 hours, and then filtered. The resultant wet product was dried for 40 hours at 45~65C to give the title compound Intermediate 8 (18.95kg: chemical purity 99%, chiral purity 100%). 1H NMR (400 MHz, DMSO-^6) delta 12.59 (s, 1H), 10.43 (s, 1H), 7.92 (d, J= 5.8 Hz, 1H), 7.29 (d, J = 2.4 Hz, 1H), 6.97 (d, J= 8.8 Hz, 1H), 6.93 (dd, J= 8.8, 2.4 Hz, 1H), 6.21 (d, J= 5.8 Hz, 1H), 5.21 (dd, J= 5.4, 1.0 Hz, 1H), 3.27 - 3.25 (m, 1H), 2.89 (t, J= 7.8 Hz, 2H), 2.51 (d, J= 8.8 Hz, 2H), 1.19 (dd, 7= 3.0, 1.0 Hz, 1H) ppm. MS: M/e 339 (M+l)+.
 

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