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Chemical Structure| 1413085-67-2 Chemical Structure| 1413085-67-2

Structure of 1413085-67-2

Chemical Structure| 1413085-67-2

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Product Details of [ 1413085-67-2 ]

CAS No. :1413085-67-2
Formula : C6H11ClN2
M.W : 146.62
SMILES Code : N#CC[C@H]1NCCC1.[H]Cl
MDL No. :N/A

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Application In Synthesis of [ 1413085-67-2 ]

* 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 [ 1413085-67-2 ]

[ 1413085-67-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 142253-50-7 ]
  • [ 1413085-67-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In methanol; at 40.0℃; Intermediate 138: ((S)-Pyrrolidin-2-yl)a hydrochlorideHCI [00484] A solution of ferf-butyl (S)-2-cyanomethylpyrrolidine-l-carboxylate(Intermediate 139, 13.0g) in methanol (130mL) and concentrated hydrochloric acid (13mL) was stirred and heated at 40C overnight. After cooling, the mixture was concentrated under vacuum and the residue was diluted with toluene and reconcentrated. Ethanol (20mL) was added and the resultant solid was collected by filtration and washed with hexane to give ((S)- pyrrolidin-2-yl)acetonitrile hydrochloride (8.0g) as a white solid.LCMS (Method D) r/t 0.50 (M+H) 111.
8.0 g With hydrogenchloride; water; In methanol; at 40.0℃; Intermediate 138: ((S)-Pyrrolidin-2-yl)acetonitrile h drochloride HCI [00409] A solution of tert-butyl (S)-2-cyanomethylpyrrolidine- 1 -carboxylate (Intermediate 139, 13. Og) in methanol (130mL) and concentrated hydrochloric acid (13mL) was stirred and heated at 40C overnight. After cooling, the mixture was concentrated under vacuum and the residue was diluted with toluene and reconcentrated. Ethanol (20mL) was added and the resultant solid was collected by filtration and washed with hexane to give ((S)- pyrrolidin-2-yl)acetonitrile hydrochloride (8.0g) as a white solid. LCMS (Method D) r/t 0.50 (M+H) 1 11.
With hydrogenchloride; water; In methanol; at 40.0℃; Step 3 : tert-butyl 3-oxopropylcarbamate [00278] To a solution of (S)-tert-butyl 2-(cyanomethyl)pyrrolidine-l-carboxylate (1.77 g, 4.45 mmol) in methanol (18 mL) was added 12N HC1 (1.8 mL). The reaction mixture was stirred at 40C overnight. The solvent was removed under reduced pressure, the resulting residue was co-evaporated with toluene twice and high vacuum to give (S)-2-(pyrrolidin-2- yl)acetonitrile hydrochloride (1.35 g) as a white solid, which was used in the next step without further purification.
 

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