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Hydrochloric Acid → Methyl 2-amino-5-fluoroisonicotinate

HRID 1802181
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인쇄 미리보기

반응식

HRID 1802181 반응식
C(OC([NH:8][C:9]1[CH:10]=[C:11]([C:16]([F:19])=[CH:17][N:18]=1)[C:12]([O:14][CH3:15])=[O:13])=O)(C)(C)C.Cl>>[NH2:8][C:9]1[CH:10]=[C:11]([C:16]([F:19])=[CH:17][N:18]=1)[C:12]([O:14][CH3:15])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 313Hydrochloric AcidHCID 67776932Methyl 2-((tert-butoxycarbonyl)amino)-5-fluoroisonicotinate

생성물 1

HCID 67777217Methyl 2-amino-5-fluoroisonicotinate수율 82.2%

반응 조건

온도
25 °C

실험 절차

A mixture of methyl 2-(tert-butoxycarbonylamino)-5-fluoroisonicotinate (1.80 g, 6.66 mmol) and hydrochloric acid (6N in ether, 40 ml, 240 mmol) is stirred for 20 hours at 25° C. The solvent is evaporated and the light brown slurry is diluted with ethyl acetate, cooled to 0° C. and adjusted to pH 8 with sat. aqueous sodium carbonate solution. The organic layer is washed with brine, dried with magnesium sulfate and the solvent is removed under reduced pressure affording methyl 2-amino-5-fluoroisonicotinate (932 mg, 82.2%) as a brown waxy solid. MS: m/z=171.0 (M+H+).

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. customThe solvent is evaporated
  2. additionthe light brown slurry is diluted with ethyl acetate
  3. temperaturecooled to 0° C.
  4. washThe organic layer is washed with brine
  5. dry with materialdried with magnesium sulfate
  6. customthe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-b9c3b27add114eac9405dc262a06f3a8
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08349824B2

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