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Diethyl Ether → HCID 86753881, 화합물

HRID 1418392
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HRID 1418392 반응식
[ClH:1].Cl.[NH2:3][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[C:5]=1[C:6]([NH2:8])=[NH:7].C1O[C:17]2([CH2:22][CH2:21][NH:20][CH2:19][CH2:18]2)OC1.CCOCC>C(O)C.Cl>[ClH:1].[ClH:1].[F:13][C:9]1[CH:10]=[CH:11][CH:12]=[C:4]2[C:5]=1[C:6]([NH2:8])=[N:7][C:17]1([CH2:22][CH2:21][NH:20][CH2:19][CH2:18]1)[NH:3]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 3283Diethyl EtherHCID 674351,4-Dioxa-8-azaspiro(4.5)decaneHCID 22008823HCID 22008823, 화합물

생성물 1

HCID 86753881HCID 86753881, 화합물수율 169.3%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of 2-amino-6-fluorobenzamidine dihydrochloride (Example C, 226 mg, 1 mmol) and 4-piperidone ethylene ketal (143 mg, 1 mmol) in dry ethanol (10 ml) was added IN HCl in ether (1 ml, 1 mmol) and the resulting mixture was heated at reflux for 36 h. The solid which separated on cooling was collected by filtration and recrystallised from ethanol to give the title compound (260 mg) as yellow crystals, m.p. 305°-307° C. (dec.).

후처리

  1. temperaturethe resulting mixture was heated
  2. temperatureat reflux for 36 h
  3. customThe solid which separated
  4. temperatureon cooling
  5. filtrationwas collected by filtration
  6. customrecrystallised from ethanol

출처 및 근거

ORD 기록
ord-8f4910a431984124ac33adb9ec8f4736
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05883102

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