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Trifluoroacetic acid → HCID 66846903, 화합물

HRID 1466680
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반응식

HRID 1466680 반응식
C(O)(C(F)(F)F)=O.[Br:8][C:9]1[S:10][C:11]([NH:23]C(=O)OC(C)(C)C)=[C:12]([C:14]2[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:15]=2[O:21][CH3:22])[N:13]=1>C(Cl)Cl.O>[Br:8][C:9]1[S:10][C:11]([NH2:23])=[C:12]([C:14]2[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:15]=2[O:21][CH3:22])[N:13]=1
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참가 물질

5

반응물 2

HCID 6422Trifluoroacetic acidHCID 66847104HCID 66847104, 화합물

생성물 1

HCID 66846903HCID 66846903, 화합물

시약·촉매·용매 2

HCID 962Water촉매HCID 6344Dichloromethane용매

실험 절차

TFA (4.0 mL) was added to a solution of tert-butyl 2-bromo-4-(5-chloro-2-methoxyphenyl)thiazol-5-ylcarbamate (360 mg, 0.86 mmol) in DCM (10 mL) and water (3 drops). The reaction mixture was stirred for 1.5 hours at room temperature and then evaporated to dryness. The residue was taken up into DCM and washed with sodium hydrogen carbonate (sat. aq.), water and brine, and concentrated under vacuum to give 2-bromo-4-(5-chloro-2-methoxyphenyl)thiazol-5-amine as an orange residue. LCMS (ESI) m+H=321.3. NMR (400 MHz, DMSO-d6): δ 7.36 (d, 1H); 7.34-7.32 (m, 1H); 7.10 (d, 1H); 3.83 (s, 3H).

후처리

  1. customevaporated to dryness
  2. washwashed with sodium hydrogen carbonate (sat. aq.), water and brine
  3. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-9a3882ad4d7143e9afaaf6397dafc11c
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999998B2

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