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Chemical Structure| 737000-78-1 Chemical Structure| 737000-78-1

Structure of 737000-78-1

Chemical Structure| 737000-78-1

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Product Details of [ 737000-78-1 ]

CAS No. :737000-78-1
Formula : C11H13N3O2
M.W : 219.24
SMILES Code : O=C(OC(C)(C)C)NC1=NC=CC(C#N)=C1
MDL No. :MFCD03791311

Safety of [ 737000-78-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H319
Precautionary Statements:P264-P270-P280-P301+P312-P305+P351+P338-P330-P337+P313-P403-P501

Application In Synthesis of [ 737000-78-1 ]

* 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 [ 737000-78-1 ]

[ 737000-78-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 737000-78-1 ]
  • [ 42182-27-4 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In dichloromethane; at 20℃; for 3h; To a solution of tert-butyl (4-cyanopyridin-2-yl)carbamate (6.5 g, 29.6 mmol) in 60 mL of DCM was added 20 mL of trifluoroacetic acid. The reaction was stirred at r.t. for 2 hrs, and then concentrated to dryness under vacuum. Aq. NaHC03 (10 mL) was added and extracted with EA (20 mL * 3). The organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated under vacuum to give 3.5 g crude of compound 2-aminoisonicotinonitrile. 1HNMR(400MHz, CDC13) : delta= 8.20 (d, J=5.3 Hz, 1H), 6.82 (dd, J=1.0, 5.3 Hz, 1H), 6.69 (s, 1H), 4.77 (br. s., 2H). MS (ESI): M/Z (M+l) 120.1.
With trifluoroacetic acid; In dichloromethane; at 20℃; for 2h; (b) 2-aminoisonicotinonitrile To a solution of tert-butyl (4-cyanopyridin-2-yl)carbamate (6.5 g, 29.6 mmol) in 60 mL of DCM was added 20 mL of trifluoroacetic acid. The reaction was stirred at r.t. for 2 hrs, and then concentrated to dryness under vacuum. Aq. NaHCO3 (10 mL) was added and extracted with EA (20 mL*3). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated under vacuum to give 3.5 g crude of compound 2-aminoisonicotinonitrile. 1HNMR (400 MHz, CDCl3): delta=8.20 (d, J=5.3 Hz, 1H), 6.82 (dd, J=1.0, 5.3 Hz, 1H), 6.69 (s, 1H), 4.77 (br. s., 2H). MS (ESI): M/Z (M+1): 120.1.
With trifluoroacetic acid; In dichloromethane; at 20℃; for 2h; To a solution of tert-butyl (4-cyanopyridin-2-yl)carbamate (6.5 g, 29.6 mmol) in 60 mL of DCM was added 20 mL of trifluoroacetic acid. The reaction was stirred at r.t. for 2 hrs, and then concentrated to dryness under vacuum. Aq. NaHC03 (10 mL) was added and extracted with EA (20 mL * 3). The organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated under vacuum to give 3.5 g crude of compound 2- aminoisonicotinonitrile. 1HNMR (400MHz, CDC13 ) : delta= 8.20 (d, J=5.3 Hz, 1H), 6.82 (dd, J=1.0, 5.3 Hz, 1H), 6.69 (s, 1H), 4.77 (br. s., 2H). MS (ESI): M/Z (M+l): 120.1.
 

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