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Chemical Structure| 305371-42-0 Chemical Structure| 305371-42-0

Structure of 305371-42-0

Chemical Structure| 305371-42-0

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Product Details of [ 305371-42-0 ]

CAS No. :305371-42-0
Formula : C12H15ClN2O4
M.W : 286.71
SMILES Code : O=C(OC)C1=C(NC(OC(C)(C)C)=O)C=NC(Cl)=C1
MDL No. :MFCD16036620

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Application In Synthesis of [ 305371-42-0 ]

* 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 [ 305371-42-0 ]

[ 305371-42-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 171178-46-4 ]
  • [ 305371-42-0 ]
YieldReaction ConditionsOperation in experiment
100% In tetrahydrofuran; Step 1: Methyl 5-[(tert-butoxy)carbonylamino]-2-chloropyridine-4-carboxylate <strong>[171178-46-4]5-[(tert-butoxy)carbonylamino]-2-chloropyridine-4-carboxylic acid</strong> (1 equivalent) was dissolved in THF and MeOH. The mixture was heated to 50 C. to completely dissolve the starting material. The solution was then cooled to 0 C., and TMSCHN2 (2 M in THF, 2 equivalents) was added. The reaction was allowed to warm to room temperature and stirred overnight. The reaction was the concentrated to yield the methyl ester (100%) as a brown solid.
  • 2
  • [ 171178-46-4 ]
  • [ 18107-18-1 ]
  • [ 305371-42-0 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogen;nickel; In methanol; hexane; chloroform; at 20℃; for 2h; 5-tert-Butoxycarbonylamino-2-chloro-isonicotinic acid, methyl ester To 5.4 g of <strong>[171178-46-4]5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid</strong> in 50 mL of methanol and 100 mL of chloroform was at 0 C. was added 15 mL of 2 M (trimethylsilyl)diazomethane in hexanes. After allowing the reaction to warm to ambient temperature and stirring for 2 hours, the solvents were removed and the crude product purified by passing through a plug of silica gel with chloroform. The product was then recrystallized from hexanes to give 5.8 g (100%) of <strong>[171178-46-4]5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid</strong>, methyl ester: mp=90-96 C. (decomposed); mass spectrum (m/e): M+H 287.1.
  • 3
  • trimethylsilyl diazomethane [ No CAS ]
  • [ 171178-46-4 ]
  • [ 305371-42-0 ]
YieldReaction ConditionsOperation in experiment
100% In methanol; chloroform; at 0 - 20℃; for 2h; To 5.4 g of <strong>[171178-46-4]5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid</strong> in 50 mL of methanol and 100 mL of chloroform was at 0C was added 15 mL of 2 M (trimethylsilyl)diazomethane in hexanes. After allowing the reaction to warm to ambient temperature and stirring for 2 hours, the solvents were removed and the crude product purified by passing through a plug of silica gel with chloroform. The product was then recrystallized from hexanes to give 5.8 g (100%) of <strong>[171178-46-4]5-tert-butoxycarbonylamino-2-chloro-isonicotinic acid</strong>, methyl ester: mp = 90-96C (decomposed); mass spectrum (m/e): M+H 287.1.
  • 4
  • [ 67-56-1 ]
  • [ 171178-46-4 ]
  • [ 305371-42-0 ]
YieldReaction ConditionsOperation in experiment
100% 5- [ (TERT-BUTOXY) CARBONYLAMINO]-2-CHLOROPYRIDINE-4-CARBOXYLIC ACID (1 equivalent) was dissolved in THF and MeOH. The mixture was heated to 50 C to completely dissolve the starting material. The solution was then cooled to 0 C, and TMSCHN2 (2 M in THF, 2 equivalents) was added. The reaction was allowed to warm to room temperature and stirred overnight. The reaction was the concentrated to yield the methyl ester (100 %) as a brown solid.
79% 5-((fe/f-butoxycarbonyl)amino)-2-chloroisonicotinic acid (Intermediate B) (4.27 g, 15 mmol, 1 equiv.) was added to a 500 mL two necked oven-dried round bottom flask equipped with a stirring bar and suspended in dichloromethane (187 mL, 0.08M) was added. 4-Dimethylamino pyridine (7.40 g, 60 mmol, 4 equiv.) was added at 22C resulting in an homogeneous solution. /V-(3-dimethylaminopropyl)-/V-ethylcarbodiimide (4.65 g, 30 mmol, 2 equiv.) was added at that temperature and the crude mixture was stirred for 3 h. Anhydrous MeOH (HPLC quality), (5.5 mL, 135 mmol, 9 equiv.) was added to the solution and the mixture was stirred for 1 h at 22C. The resulting mixture was heated to reflux using an aluminium heating block for 72 h. TLC (EtOAc:MeOH 90:10 %v/v) showed complete conversion of Intermediate B into Intermediate C. The reaction was permitted to reach to 22C and volatiles were removed under reduced pressure. Dichloromethane (150 mL) was added to the residue until complete solution was achieved and the mixture was transferred to a separating funnel, washed with H2O (1 x 70 mL), HCI 1 M (2 x 50 mL) and saturated NaCI solution (1 x 50 mL). The organic phase was dried with Na2S04 and filtered through a pad of Na2S04 on a filter plate. The solvent was removed under reduced pressure giving a brown solid, which was purified by automated flash chromatography (Heptane:EtOAc, product elution with EtOAc 100%v/v) giving methyl 5-((fe/f-butoxycarbonyl)amino)-2-chloroisonicotinate as a pale yellow solid (4.04 g, 79% yield). Purity: 99.4% (UPLC-A); mp: 90.0-95.8 C; 1H- NMR (CDCI3), 5(ppm): 9.68 (bs, NH), 9.49 (s, 1 H), 7.73(s, 1 H), 7.20 (s, 1 H), 3.91 (s, 3H), 1.47 (s, 9H); LR-MS (ESI+): m/z= 287.1 Da [M+H]+, calcd. for CI2HI5CIN204: 286.2
 

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