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Chemical Structure| 184002-61-7 Chemical Structure| 184002-61-7

Structure of 184002-61-7

Chemical Structure| 184002-61-7

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Product Details of [ 184002-61-7 ]

CAS No. :184002-61-7
Formula : C9H19N3O3
M.W : 217.27
SMILES Code : O=C(OC(C)(C)C)NC(C)(C)C(NN)=O
English Name :tert-Butyl (1-hydrazinyl-2-methyl-1-oxopropan-2-yl)carbamate

Safety of [ 184002-61-7 ]

Application In Synthesis of [ 184002-61-7 ]

* 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 [ 184002-61-7 ]

[ 184002-61-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 84758-55-4 ]
  • [ 184002-61-7 ]
YieldReaction ConditionsOperation in experiment
72% With hydrazine In methanol at 55℃; for 24h;
With hydrazine hydrate In isopropyl alcohol 17.2 Step 2: Step 2: tert-Butyl (2-hydrazino-1,1-dimethyl-2-oxoethyl)carbamate (P2) To a solution of P1 in 2-Propanol (0.56 M) was added hydrazine monohydrate (10 eq) and the mixture was stirred overnight at 90° C. Volatiles were removed under high vacuum and the obtained crude was used as such in the next step. MS (ES) C9H19N3O3 requires: 217, found: 240 (M+Na)+.
With hydrazine In isopropyl alcohol at 90℃; 17.2 Step 2: tert-Butyl (2-hydrazino-1,1-dimethyl-2-oxoethyl)carbamate (P2) To a solution of P1 in 2-Propanol (0.56 M) was added hydrazine monohydrate (10 eq) and the mixture was stirred overnight at 90° C. Volatiles were removed under high vacuum and the obtained crude was used as such in the next step. MS (ES) C9H19N3O3 requires: 217, found: 240 (M+Na)+.
  • 2
  • [ 1453-50-5 ]
  • [ 184002-61-7 ]
  • [ 950605-21-7 ]
YieldReaction ConditionsOperation in experiment
46% Stage #1: N-cyclopropylcyclopropanecarboxamide With methyl trifluoromethanesulfonate at 60℃; for 0.5h; Stage #2: tert-butyl (1-hydrazinyl-2-methyl-1-oxopropan-2-yl)carbamate With triethylamine In toluene at 60 - 100℃; for 3h; tert-Butyl [2-(4,5-Dicyclopropyl-4H-1,2,4-triazol-3-yl)-propan-2-yl]carbamate (17) A mixture of 8a (500 mg,3.99 mmol) and methyl trifluoromethanesulfonate (452 μL,3.99 mmol) was stirred at 60°C for 30 min. Toluene(9 mL), Et3N (557 μL, 3.99 mmol) and tert-butyl(1-hydrazinyl-2-methyl-1-oxopropan-2-yl) carbamate (16,723 mg, 3.33 mmol, CAS No.; 184002-61-7) were added andthe reaction mixture was stirred at 60°C for 2 h and 100°C for1 h. CHCl3 and saturated aqueous sodium hydrogen carbonatesolution were added to the mixture, and the organic layer wasseparated and washed with brine, dried over MgSO4, filteredand concentrated in vacuo. The residue was purified by columnchromatography on silica gel (CHCl3-MeOH) to give thetitle compound 17 (464 mg, 1.51 mmol, 46%) as a white solid.1H-NMR (300 MHz, CDCl3) δ: 0.94-1.24 (8H, m), 1.35 (9H,br s), 1.78 (6H, s), 1.88-2.01 (1H, m), 3.00-3.13 (1H, m), 5.28(1H, br s). ESI-MS m/z: 307 [M + H]+.
 

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