تفاعل #2286311

ord-a608a851627a4a35a1201585d593020e

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
CC(C)c1cc(C(C#N)c2c(Cl)cc(N)cc2Cl)nnc1Cl
(4-amino-2,6-dichloro-phenyl)-(6-chloro-5-isopropyl-pyridazin-3-yl)-acetonitrile
CC(C)c1cc(C(C#N)c2c(Cl)cc(N)cc2Cl)nnc1Cl
(4-Amino-2,6-dichloro-phenyl)-(6-chloro-5-isopropyl-pyridazin-3-yl)-acetonitrile
O
water
Cl
hydrochloric acid
CC(C)c1cc(Cc2c(Cl)cc(N)cc2Cl)n[nH]c1=O
6-(4-amino-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-one
المردود 76.0%
CC(C)c1cc(Cc2c(Cl)cc(N)cc2Cl)n[nH]c1=O
6-(4-Amino-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-one
المردود 76.0%

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAt this time, the reaction was cooled to room temperature
  2. 2
    workup.ADDITIONthe mixture was poured onto water (250 mL)
  3. 3
    ترشيحThe resulting solids were filtered
  4. 4
    غسيلwashed with water and petroleum ether
  5. 5
    أخرىThe solids were collected
  6. 6
    workup.DISSOLUTIONdissolved in hot ethyl acetate
  7. 7
    workup.ADDITIONSilica gel 60 (70-230 mesh) was added
  8. 8
    تركيزthe solvent was concentrated under vacuum
  9. 9
    أخرىThe resulting mixture was purified by flash chromatography (Biotage 75S)
  10. 10
    غسيلeluted with 40% ethyl acetate in hexanes to 50% ethyl acetate in hexanes containing 0.5% glacial acetic acid
  11. 11
    أخرىThe desired fractions were collected
  12. 12
    تركيزconcentrated under vacuum
  13. 13
    أخرىto afford a solid which
  14. 14
    أخرىwas dried under high vacuum

الإجراء التجريبي

A mixture of (4-amino-2,6-dichloro-phenyl)-(6-chloro-5-isopropyl-pyridazin-3-yl)-acetonitrile (45) (6.98 g, 19.63 mmol), water (30 mL), concentrated hydrochloric acid (120 mL) and glacial acetic acid (30 mL) was heated to 120° C. for 24 h. At this time, the reaction was cooled to room temperature and the mixture was poured onto water (250 mL). The pH was made neutral (pH=7) by the addition of a 4N aqueous sodium hydroxide solution. The suspension was placed in the freezer for 15 min. The resulting solids were filtered and washed with water and petroleum ether. The solids were collected and dissolved in hot ethyl acetate. Silica gel 60 (70-230 mesh) was added and the solvent was concentrated under vacuum. The resulting mixture was purified by flash chromatography (Biotage 75S) using silica gel eluted with 40% ethyl acetate in hexanes to 50% ethyl acetate in hexanes containing 0.5% glacial acetic acid. The desired fractions were collected and concentrated under vacuum to afford a solid which was dried under high vacuum to afford 6-(4-amino-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-one (46) (4.65 g, 76%) as an off-white solid; LRMS for C14H15Cl2N3O (M+H) m/z=312. Molecular Weight=312.2012; Exact Mass=311.0592

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE046024E1uspto-grants-2016_06