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Chemical Structure| 937046-97-4 Chemical Structure| 937046-97-4

Structure of 937046-97-4

Chemical Structure| 937046-97-4

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Product Details of [ 937046-97-4 ]

CAS No. :937046-97-4
Formula : C5H6ClN3
M.W : 143.57
SMILES Code : N#CC1=CC=CN1N.[H]Cl
MDL No. :MFCD13191739
InChI Key :OQTSWPFWLRHRAN-UHFFFAOYSA-N
Pubchem ID :50990937

Safety of [ 937046-97-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331
Precautionary Statements:P261-P280-P301+P310-P311
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 937046-97-4 ]

* 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 [ 937046-97-4 ]

[ 937046-97-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 937046-96-3 ]
  • [ 937046-97-4 ]
YieldReaction ConditionsOperation in experiment
97% With hydrogenchloride; In water; ethyl acetate; at 0℃; for 0.5h;Large scale; Add 1000g of Compound II (4.83mol, 1.0eq) and 3L of anhydrous ethyl acetate to a 20L three-necked bottle, stir to dissolve, and lower the temperature to 0 C to obtain the reaction solution, which is ready for use 5L of an ethyl acetate solution with a concentration of 1 mol / l was prepared with acid as the solute and ethyl acetate as the solvent, and it was completely added to the prepared reaction solution.Keeping the reaction at 0 C, a large amount of white solid was observed for 30 min. After the reaction was monitored by TLC, suction filtration was performed, and the residue was washed with anhydrous ethyl acetate and dried in vacuo. 680 g of white solid was obtained as intermediate III (1-amino-(9ci)-1H-pyrrole-2-carbonitrile hydrochloride).The purity of this intermediate III was 99%, and the yield was 97%.
85% With hydrogenchloride; In 1,4-dioxane; at 0 - 20℃; for 5.5h; A 3L, 3-neck RB flask was fitted with a mechanical stirrer, nitrogen inlet, thermocouple/JKEM thermocontroller, addition funnel and ice water cooling bath. (2- Cyano-pyrrol-1-yl)-carbamic acid, tert-butyl ester (85 g, 0.41 mol) was added and dissolved with 1 ,4-dioxane (400 ml_), then the stirred orange solution was cooled to 0 0C and HCI/dioxane (4N, 820 ml_, 8 eq.) was slowly added from the addition funnel, maintaining an internal temperature below 5 0C. After -30 minutes the solution became cloudy and stirring (at) room temperature was continued for 5 hours; the reaction was monitored for completion by TLC (silica gel, GHLF, 1 :3 EtOAc/hexane, UV; Note: the free base may be observed as a high-Rf spot and can be misinterpreted as incomplete reaction). The reaction mixture was diluted with diethyl ether (2L) and the precipitated solids were collected by suction filtration and washed with ether (1 L). Drying (vacuum oven (at) 500C) afforded the desired product as 50.5 g (85%) of a tan solid. 1H-NMR (CD3OD): 87.05 (dd, 1H, J =2.8, 1.9 Hz ), 6.75 (dd, 1H, J =1.8, 4.2 Hz), 6.13 (dd, 1H, J =2.8, 4.4 Hz ), 5.08 (s, 3H, NH3+); MS: GC/MS, m/z= 108.2 [M+H].
85% With hydrogenchloride; In 1,4-dioxane; at 0 - 20℃; for 5.5h; A 3L, 3-neck RB flask was fitted with a mechanical stirrer, nitrogen inlet, thermocouple/JKEM thermocontroUer, addition funnel and ice water cooling bath. (2-Cyano-pyrrol-l-yl)-carbamic acid, tert-butyl ester (85 g, 0.41 mol) was added and dissolved with 1,4-dioxane (400 mL), then the stirred orange solution was cooled to 0 0C and <n="164"/>HCl/dioxane (4N, 820 mL, 8 eq.) was slowly added from the addition funnel, maintaining an internal temperature below 5 0C. After -30 minutes the solution became cloudy and stirring @ room temperature was continued for 5 hours; the reaction was monitored for completion by TLC (silica gel, GHLF, 1:3 EtOAc/hexane, UV; Note: the free base may be observed as a high-Rf spot and can be misinterpreted as incomplete reaction). The reaction mixture was diluted with diethyl ether (2L). and the precipitated solids were collected by suction filtration and washed with ether (IL). Drying (vacuum oven @ 5O0C) afforded the desired product as 50.5 g (85%) of a tan solid. 1H-NMR (CD3OD): 67.05 (dd, IH, / =2.8, 1.9 Hz ), 6.75 (dd, IH, J =1.8, 4.2 Hz), 6.13 (dd, IH, J =2.8, 4.4 Hz ), 5.08 (s, 3H, NH3+); MS: GCMS, m/z= 108.2 [M+H].
 

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