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HCID 21104706, 화합물 → HCID 21104576, 화합물

HRID 1354233
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반응식

HRID 1354233 반응식
[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][NH:12][CH2:13][C:14]3[CH2:19][N:18](NC(OC(C)(C)C)=O)[CH2:17][CH2:16][CH:15]=3)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1>C(O)(C(F)(F)F)=O>[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][NH:12][CH2:13][C:14]3[CH2:19][NH:18][CH2:17][CH2:16][CH:15]=3)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 21104706HCID 21104706, 화합물

생성물 1

HCID 21104576HCID 21104576, 화합물

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of tert-butyl 5-{[(2,3-dihydro-benzo[1,4]-dioxin-6-ylmethyl)-amino]-methyl}-3,6-dihydro-2H-pyridine-1-carbamate (0.16 g, 0.44 mmol) in TFA (3 ml) was stirred at room temperature for 30 minutes, concentrated and taken up in saturated bicarbonate solution (30 ml) and dichloromethane (30 ml). The aqueous phase was extracted with dichloromethane (2×30 ml) and the combined organic phases were washed with saturated sodium chloride solution, dried over MgSO4 and concentrated.

후처리

  1. concentrationconcentrated
  2. extractionThe aqueous phase was extracted with dichloromethane (2×30 ml)
  3. washthe combined organic phases were washed with saturated sodium chloride solution
  • dry with materialdried over MgSO4
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-7451420421c046709b49d608bad220da
    출처 데이터셋
    uspto-grants-2007_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07223776B2

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