Hydrochloric Acid → 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)one hydrochloride

HRID 247271

반응식

HRID 247271 반응식
Cl.[CH3:2][N:3]1C[CH2:6][CH:5]([O:8][C:9]2[C:14]([C:15]([O-:17])=O)=[CH:13][CH:12]=[CH:11][N:10]=2)[CH2:4]1.[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:38]([Cl:42])(Cl)(Cl)[Cl:39]>C(Cl)(Cl)Cl.C(O)C>[ClH:39].[Cl:42][CH2:38][CH2:6][CH:5]1[CH2:4][N:3]([CH3:2])[C:15](=[O:17])[C:14]2[CH:13]=[CH:12][CH:11]=[N:10][C:9]=2[O:8]1

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 5943Carbon TetrachlorideHCID 11776TriphenylphosphineHCID 23718944Sodium 2-[(1-methyl-3-pyrrolidinyl)oxy]-3-pyridinecarboxylate

생성물 1

HCID 137264372-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)one hydrochloride

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6212Chloroform용매

실험 절차

Hydrogen chloride gas was bubbled into a suspension of 150 g (0.61 mole) of sodium 2-[(1-methyl-3-pyrrolidinyl)oxy]-3-pyridinecarboxylate in 1 liter of chloroform until a pH of 6 was reached. To the stirred mixture was added 350 g (1.34 mole) of triphenylphosphine and 350 g (2.3 mole) of carbon tetrachloride and the resulting cloudy solution was stirred at reflux for 1.5 hr. About 100 ml of ethanol was added and the heat removed. The solution was stirred for 1 hour while cooling and 200 ml of isooctane was added. The solution was extracted 4 times with a total of 800 ml of dilute hydrochloric acid. The acid extracts were combined, made basic with sodium hydroxide and extracted with chloroform. The chloroform layer was separated and dried over sodium sulfate and concentrated. The residue was dissolved in a mixture of 500 ml each of isopropyl alcohol and isopropyl ether and acidified with ethereal hydrogen chloride. The resulting crystals weighed 82 g (49%). A portion was recrystallized from isopropyl alcohol, m.p. 149°-153° C.

후처리

  1. temperatureat reflux for 1.5 hr
  2. customthe heat removed
  3. stirringThe solution was stirred for 1 hour
  4. temperaturewhile cooling
  5. addition200 ml of isooctane was added
  6. extractionThe solution was extracted 4 times with a total of 800 ml of dilute hydrochloric acid
  7. extractionextracted with chloroform
  8. customThe chloroform layer was separated
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated
  11. dissolutionThe residue was dissolved in a mixture of 500 ml each of isopropyl alcohol and isopropyl ether
  12. customA portion was recrystallized from isopropyl alcohol, m.p. 149°-153° C.

출처 및 근거

ORD 기록
ord-970ba48e7bf84eebaf1a01268f68547e
출처 데이터셋
uspto-grants-1987_11
특허 번호
US04705853

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