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HCID 18919774, 화합물 → HCID 18919904, 화합물

HRID 1291179
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HRID 1291179 반응식
[Cl:1][C:2]1[CH:24]=[CH:23][C:5]([C:6]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([CH2:15][C:16]3[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][CH:17]=3)[CH2:11][CH2:10]2)=[O:7])=[CH:4][CH:3]=1>CCOCC>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH:9]2[CH2:10][CH2:11][N:12]([CH2:15][C:16]3[CH:17]=[CH:18][C:19]([Br:22])=[CH:20][CH:21]=3)[CH2:13][CH2:14]2)=[O:7])=[CH:23][CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 18919774HCID 18919774, 화합물

생성물 1

HCID 18919904HCID 18919904, 화합물수율 153.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

0.204 g (0.00055 mol) of 1-(4-bromo-benzyl)-piperidin-4-yl 4-chloro-benzoate was dissolved in 15 ml of ether, filtered, diluted with 0.75 ml of methanol and treated with 5ml of 1N ethereal HCI. The separated precipitate was filtered off and dried. 0.188 g (83.6%) of 1-(4-bromo-benzyl)-piperidin-4-yl 4-chloro-benzoate hydrochloride (1:1) was obtained as white crystals; m.p. 240°-242°.

후처리

  1. filtrationfiltered
  2. additiondiluted with 0.75 ml of methanol
  3. additiontreated with 5ml of 1N ethereal HCI
  4. filtration
The separated precipitate was filtered off
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-3ec2cd5e79e64bee8bd19a69eb75d81a
    출처 데이터셋
    uspto-grants-1998_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05753679

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