تفاعل #4932

ord-7df9808670ba4f2b81ba407bc9a2e80e

معادلة التفاعل

CN1CC(CCCl)Oc2ncccc2C1=O.Cl
2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-one hydrochloride
C1CCNC1
pyrrolidine
[Na+].[OH-]
sodium hydroxide
O=C(O)/C=C/C(=O)O
fumaric acid
CN1CC(CCN2CCCC2)Oc2ncccc2C1=O.O=C(O)/C=C/C(=O)O
2,3-Dihydro-4-methyl-2-[2-(1-pyrrolidinyl)ethyl]pyrido[3,2-f][1,4]-oxazepin-5(4H)-one fumarate

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe solution was cooled to room temperature
  2. 2
    استخلاصThe resulting solution was extracted with chloroform (3×30 ml)
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    workup.ADDITIONwas added
  5. 5
    ترشيحThe solution was filtered hot
  6. 6
    درجة الحرارةthe filtrate cooled to 20° C. for several hours
  7. 7
    أخرىThe resulting crystals, 14 g (47.8%) were collected
  8. 8
    أخرىrecrystallized from isopropyl alcohol, m.p. 147°-149° C.

الإجراء التجريبي

A sample of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-one hydrochloride, 16 g (0.058 mole), was dissolved in 65 ml of pyrrolidine. The stirred solution was heated to 80° C. for 3 hr. The solution was cooled to room temperature and dilute sodium hydroxide solution (50 ml) was added. The resulting solution was extracted with chloroform (3×30 ml) and concentrated in vacuo. The residue was taken up in boiling isopropyl alcohol (500 ml/ and fumaric acid (9.2 g, 0.079 mole) was added. The solution was filtered hot and the filtrate cooled to 20° C. for several hours. The resulting crystals, 14 g (47.8%) were collected and recrystallized from isopropyl alcohol, m.p. 147°-149° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727152uspto-grants-1988_02