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Hydrochloric Acid → N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride

HRID 1085838
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인쇄 미리보기

반응식

HRID 1085838 반응식
[C:1]1([C:7]2[C:8]([C:12]([NH:14][CH2:15][CH2:16][NH:17]C(=O)OC(C)(C)C)=[O:13])=[N:9][O:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.FC(F)(F)C(O)=O.[ClH:32]>>[ClH:32].[NH2:17][CH2:16][CH2:15][NH:14][C:12]([C:8]1[C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:11][O:10][N:9]=1)=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 54501153HCID 54501153, 화합물

생성물 1

HCID 19768554N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride수율 94.1%

실험 절차

5.0 % (15.1 mmol) of t-butyl [2-(4-phenyl-3-isoxazolecarboxamido)ethyl]carbamate were stirred at room temperature for 16 hours with trifluoroacetic acid analogously to Example 13. After concentration there was obtained a residue which was converted into the hydrochloride. Recrystallization of the crude product from methanol/ether yielded 3.B g (94.1%) of N-(2-aminoethyl)4-phenyl-3-isoxazolecarboxamide hydrochloride as white crystals, melting point 211°-212°.

후처리

  1. concentrationAfter concentration
  2. customthere was obtained a residue which
  3. customRecrystallization of the crude product from methanol/ether

출처 및 근거

ORD 기록
ord-79ea207a1c7d4b11a1b293df1f2f5fcd
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05011849

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