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ChemicalBook CAS DataBase List exo-3-Boc-6-cyano-3-azabicyclo[3.1.0]hexane

exo-3-Boc-6-cyano-3-azabicyclo[3.1.0]hexane synthesis

3synthesis methods
tert-butyl (1R,5S,6r)-6-carbamoyl-3-azabicyclo[3.1.0]hexane-3-carboxylate

1269429-62-0
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exo-3-Boc-6-cyano-3-azabicyclo[3.1.0]hexane

871239-62-2
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Yield:871239-62-2 96%

Reaction Conditions:

with isocyanuric acid in N,N-dimethyl-formamide at 20; for 2 h;

Steps:

4.2 Step 2: Synthesis of tert-butyl (lR,5S,6r)-6-cyano-3-azabicyclo[3.1.0]hexane-3- carboxylate

To a 50-mL round-bottom flask was added tert-butyl (lS,5R)-6-carbamoyl-3- azabicyclo[3.1.0]hexane-3-carboxylate (1.00 g, 4.42 mmol, 1 equiv) and cyanuric acid (815 mg, 4.42 mmol, 1 equiv) in DMF (17 mL). The reaction was stirred for 2 hours at room (0434) temperature. After 2 hours, the reaction was diluted with water and extracted 3 times with i- PrOAc. The organic layer was then washed 2 times with water and then brine, dried over a2S04, and concentrated under vacuum to afford tert-butyl (lS,5R)-6-cyano-3-azabicyclo [3.1.0]hexane-3-carboxylate as a clear yellow oil which crystallized over time (879 mg, 96% yield).

References:

WO2018/162607,2018,A1 Location in patent:Paragraph 0243; 0244

134575-37-4 Synthesis
(1R,5S,6r)-3-tert-butyl 6-ethyl 3-azabicyclo[3.1.0]hexane-3,6-dicarboxylate

134575-37-4
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exo-3-Boc-6-cyano-3-azabicyclo[3.1.0]hexane

871239-62-2
26 suppliers
inquiry

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