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Chemical Structure| 6610-31-7 Chemical Structure| 6610-31-7

Structure of 6610-31-7

Chemical Structure| 6610-31-7

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Product Details of [ 6610-31-7 ]

CAS No. :6610-31-7
Formula : C5H13N3S
M.W : 147.24
SMILES Code : NNC(NCCCC)=S
MDL No. :MFCD00041307

Safety of [ 6610-31-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P501-P261-P270-P271-P264-P280-P362+P364-P301+P312+P330-P302+P352+P312-P304+P340+P312

Application In Synthesis of [ 6610-31-7 ]

* 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 [ 6610-31-7 ]

[ 6610-31-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15855-06-8 ]
  • [ 6610-31-7 ]
  • [ 1220708-72-4 ]
YieldReaction ConditionsOperation in experiment
83% To a stirred suspension of <strong>[15855-06-8]2-chloro-6-methoxyisonicotinic acid</strong> (0.94 g, 5.0 mmol) in dioxane (10 ml) the title compound of Preparation 1 (0.74 g, 5.0 mmol) was added. To the suspension thus obtained POCI3 (1.40 ml, 15.1 mmol) was added dropwise at room temperature. The mixture was stirred at 70C for16h. It was poured onto a mixture of a 2M aqueous solution of sodium hydroxide (50 ml) and ice (50 ml). The solid obtained was filtered, washed with water and hexane and dried to yield 1.23 g (83%) of the title compound.LRMS: m/z 299 (M+1)+ Retention time: 3.61 min (method A) 1H NMR (200 MHz, DMSO-D6) delta ppm 0.9 (t, J=7.2 Hz, 3 H) 1.4 (m, 2 H) 1.6 (m, 2 H) 3.3 (m, 2 H) 3.9 (s, 3 H) 7.1 (d, J=1.2 Hz, 1 H) 7.4 (d, =1.2 Hz, 1 H) 8.4 (t, J=6.1 Hz, 1 H)
83% PREPARATION 8 N-butyl-5-(2-chloro-6-methoxypyridin-4-yl)-1,3,4-thiadiazol-2-amine To a stirred suspension of <strong>[15855-06-8]2-chloro-6-methoxyisonicotinic acid</strong> (0.94 g, 5.0 mmol) in dioxane (10 ml) the title compound of Preparation 1 (0.74 g, 5.0 mmol) was added. To the suspension thus obtained POCl3 (1.40 ml, 15.1 mmol) was added dropwise at room temperature. The mixture was stirred at 70C for16h. It was poured onto a mixture of a 2M aqueous solution of sodium hydroxide (50 ml) and ice (50 ml). The solid obtained was filtered, washed with water and hexane and dried to yield 1.23 g (83%) of the title compound. LRMS: m/z 299 (M+1)+ Retention time: 3.61 min (method A) 1H NMR (200 MHz, DMSO-D6) delta ppm 0.9 (t, J=7.2 Hz, 3 H) 1.4 (m, 2 H) 1.6 (m, 2 H) 3.3 (m, 2 H) 3.9 (s, 3 H) 7.1 (d, J=1.2 Hz, 1 H) 7.4 (d, J=1.2 Hz, 1 H) 8.4 (t, J=6.1 Hz, 1 H)
 

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