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Chemical Structure| 735241-98-2 Chemical Structure| 735241-98-2

Structure of 735241-98-2

Chemical Structure| 735241-98-2

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Product Details of [ 735241-98-2 ]

CAS No. :735241-98-2
Formula : C5H7ClN2
M.W : 130.58
SMILES Code : CN1N=CC(CCl)=C1
MDL No. :MFCD09859328
InChI Key :GPYMVNVREOOVEQ-UHFFFAOYSA-N
Pubchem ID :21698362

Safety of [ 735241-98-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 735241-98-2 ]

* 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 [ 735241-98-2 ]

[ 735241-98-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 112029-98-8 ]
  • [ 735241-98-2 ]
YieldReaction ConditionsOperation in experiment
100% With thionyl chloride; In dichloromethane; at 0 - 20℃; for 3h; To a solution of <strong>[112029-98-8](1-methyl-1H-pyrazol-4-yl)methanol</strong> (1.29 g, 11.5 mmol) (prepared from Intermediate 3 Step A) in methylene chloride (4 mL) at 0° C. was added thionyl chloride (4 mL, 50 mmol). The solution was stirred at room temperature for 3 h. Concentration under reduced pressure gave 1.50 g (100percent yield) of the desired product as white solid, which was used for the next step directly.
86% With thionyl chloride; In dichloromethane; toluene; at 20℃; for 1h; Into a solution of <strong>[112029-98-8](1-methyl-1H-pyrazol-4-yl)methanol</strong> (790 mg, 7.04 mmol) in DCM (2.6 mL) was added a solution of thionyl chloride (1.28 mL, 17.6 mmol) in toluene (3.50 mL) drop wise. The reaction mixture was then stirred at rt for lh. Upon completion, the reaction mixture was concentrated to afford the titled compound as an off white solid (790 mg, 86percent). 1H NMR (400 MHz, CDC13) delta 7.78 (s, 1H), 7.63 (s, 1H), 4.56 (s, 2H), 4.17 (s, 3H).
With thionyl chloride; In dichloromethane; touluene; at 20℃; for 1h; D604-(Chloromethyl)-l-methyI-lH-pyrazoleTo a solution of (1 -Methyl- lH-pyrazol-4-yI)methanoI (1.1 g, 9.81 mmol) indichloromethane (5.00 ml) was added thionyl chloride (2.0 ml, 27.4 mmol) in toluene (5.0 mL) dropwise. The reaction mixture was stirred for 1 hr at rt, concentrated to afford the title product (1.34 g) as a white solid, which was used in next reaction without purification.
With thionyl chloride; In dichloromethane; for 1h;Cooling with ice; Intermediate 70 (160mg, 1 eq.) was dissolved in re-distilled dichloromethane, and dichlorosulfoxide (310 mul, 3 eq.) was added under ice bath. The mixture was reacted for 1 h, evaporated to remove solvent. The product was directly used in the next step without purification

 

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