반응 #4932

ord-7df9808670ba4f2b81ba407bc9a2e80e

반응 방정식

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

반응 조건

온도
80°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The solution was cooled to room temperature
  2. 2
    추출The resulting solution was extracted with chloroform (3×30 ml)
  3. 3
    농축concentrated in vacuo
  4. 4
    workup.ADDITIONwas added
  5. 5
    여과The solution was filtered hot
  6. 6
    온도the filtrate cooled to 20° C. for several hours
  7. 7
    기타The resulting crystals, 14 g (47.8%) were collected
  8. 8
    기타recrystallized from isopropyl alcohol, m.p. 147°-149° C.

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04727152uspto-grants-1988_02