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Chemical Structure| 120747-86-6 Chemical Structure| 120747-86-6

Structure of 120747-86-6

Chemical Structure| 120747-86-6

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Product Details of [ 120747-86-6 ]

CAS No. :120747-86-6
Formula : C5H7Cl2N3
M.W : 180.04
SMILES Code : ClCC1=CN=C(N)N=C1.[H]Cl
MDL No. :MFCD09056752

Safety of [ 120747-86-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H350
Precautionary Statements:P201-P202-P281-P308+P313-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 120747-86-6 ]

* 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 [ 120747-86-6 ]

[ 120747-86-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 120747-85-5 ]
  • [ 120747-86-6 ]
YieldReaction ConditionsOperation in experiment
52% With thionyl chloride; In dichloromethane; at 0 - 20℃; A slurry of alcohol (31 g, 0.25 mol) from Preparative Example 400, Step A in CH2Cl2 (500 mL) was cooled to 0 C. and slowly treated with SOCl2 (55 mL, 0.74 mol over 30 minutes). The reaction was then stirred overnight at 20 C. The material was concentrated, slurried in acetone, and then filtered. The resulting beige solid was dried overnight in vacuo (38.4 g, 52%, HCl salt).
52% With thionyl chloride; In dichloromethane; at 0 - 20℃; A slurry of alcohol (31 g, 0.25 mol) from Preparative Example 216, Step A in CH2CI2 (500 mL) was cooled to 0 C and slowly treated with SOCI2 (55mL, 0.74 mol over 30 minutes). The reaction was then stirred overnight at 20 C. The material was concentrated, slurried in acetone, and then filtered. The resulting beige solid was dried overnight in vacuo (38.4g, 52%, HCI salt).
With thionyl chloride; In dichloromethane; at 0 - 20℃; for 16h; To a stirred suspension of 130 (500 mg, 4 mmol) in DCM (10 mL) was added SOd2 (1 mL) drop wise atO C. After completion of the addition, the reaction mixture was allowed to RTforl6 h. The reaction mixture was concentrated under reduced pressure to get 290 mg of crude 131 as HCI salt. The crude compound was as such taken for next step without any further purification. To a stirred solution of 6-003 (582 mg, 2 mmol) in DMF (10 mL) was added 131 (290 mg, crude, 2 mmol) and K2C03 (828 mg,6 mmol) at RT. The reaction mixture was irradiated under microwave at 80 C for 1 h. The progress of the reaction was monitored by TLC. The solvent was removed under reduced pressure to get the crude material. The crude compound was purified by Grace Purification system [C-18 column with 0.01 % HCOOH in water and acetonitrile] to afford 500 mg of crude 6-225. The crude compound was purified by prep. HPLC purification to get 6-225 (60 mg, 4 % two steps) as a white solid. 1H NMR (400 MHz,DMSO-d6): O 9.03 (brs, 1 H), 8.53 (brd, J = 7.8 Hz, 1H), 8.31 (s, 2H), 7.35- 7.30 (d, J = 7.3 Hz, 1H),7.23 (d, J= 7.3 Hz, 1H), 7.09-6.84 (m, 2H), 5.13-4.85 (m, 4H), 4.37-4.22 (m, 1H), 2.43 (s, 3H), 2.11(qd, J = 13.3, 6.3 Hz, 1 H), 0.92 (d, J = 6.8 Hz, 3H), 0.90 (d, J = 6.8 Hz, 3HLC-MS: m/z 399.22 [M+H].HPLC purity: 94.03% (220 nm) and chiral HPLC purity is 98.99% (229 nm).
 

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