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Chemical Structure| 1322752-29-3 Chemical Structure| 1322752-29-3

Structure of 1322752-29-3

Chemical Structure| 1322752-29-3

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Product Details of [ 1322752-29-3 ]

CAS No. :1322752-29-3
Formula : C6H3ClN2S2
M.W : 202.68
SMILES Code : S=C(N1)SC2=C1C=NC(Cl)=C2

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Application In Synthesis of [ 1322752-29-3 ]

* 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 [ 1322752-29-3 ]

[ 1322752-29-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7321-93-9 ]
  • [ 140-89-6 ]
  • [ 1322752-29-3 ]
YieldReaction ConditionsOperation in experiment
86.6% With pyridine; In N,N-dimethyl-formamide; at 150℃; for 8h; Step-1: Synthesis of 6-chloro thiazolo[4,5-c]pyridine-2(3H)-thione Using the same reaction conditions as described in step 1 of example 1, 4,6- dichloropyridin-3-amine (1.3 g, 7 mmol) was cyclised using potassium ethyl xanthate (2.55 g, 15 mmol) in DMF (25mL) at 150C for 8h to afford the title compound (1.3 g, 86.6 %) as a light brown solid. 1HNMR (400 MHz, DMSO-d6): delta 14.2-14.0 (b, 1H), 8.274 (s, 1H), 7.931 (s, 1H); LCMS: 100%, m/z = 201.3 (M+l)+.
86.6% In N,N-dimethyl-formamide; at 150℃; for 8h; Using the same reaction conditions as described in step 1 of example 1, <strong>[7321-93-9]4,6-dichloropyridin-3-amine</strong> (1.3 g, 7 mmol) was cyclised using potassium ethyl xanthate (2.55 g, 15 mmol) in DMF (25 mL) at 150 C. for 8 h to afford the title compound (1.3 g, 86.6%) as a light brown solid. 1HNMR (400 MHz, DMSO-d6): delta 14.2-14.0 (b, 1H), 8.274 (s, 1H), 7.931 (s, 1H); LCMS: 100%, m/z=201.3 (M+1)+. A solution of 2-aminopyridin-3-ol (5.0 g, 45.45 mmol) and potassium ethyl xanthate (8.0 g, 49.99 mmol) in pyridine (50 mL) was heated at 1100 C. overnight. The reaction mixture was cooled to 00 C., added ice water and acidified with Conc. HC1. The solid was filtered and dried under vacuum to afford the title compound (6.0 g, 86.95%). 10206] ?HNMR (DMSO-d5, 300 MHz): oe 8.24-8.22 (d, 1H), 7.90-7.87 (d, 1H), 7.30-7.26 (m, 1H). LCMS: mlz:153.0 (M+1).
72% In N,N-dimethyl-formamide; at 130℃;Inert atmosphere; A mixture of <strong>[7321-93-9]4,6-dichloropyridin-3-amine</strong> (8.0 g, 49.08 mmol) and potassium O-ethyl carbonodithioate (15.7 g, 98.16 mmol) in DMF (30 mL) was stirred overnight at 130 °C under a nitrogen atmosphere. The mixture was cooled to rt and 1M HCl (200 mL) was added dropwise. The mixture was stirred for 10 min at rt. The solids were filtered, and the filter cake was washed with water and dried under vacuum to give 6-chlorothiazolo[4,5-c]pyridine- 2(3H)-thione (7.2 g, 72percent) as a yellow solid.
 

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