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Trifluoroacetic acid → 4-Chloro-5-iodo-2-methoxypyridine

HRID 1498160
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HRID 1498160 반응식
[Cl:1][C:2]1[C:7]([I:8])=[CH:6][N:5]=[C:4](N)[CH:3]=1.[C:10](O)(C(F)(F)F)=[O:11].N(OC(C)(C)C)=O>CO>[Cl:1][C:2]1[C:7]([I:8])=[CH:6][N:5]=[C:4]([O:11][CH3:10])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 10906Tert-Butyl nitriteHCID 219491214-Chloro-5-iodopyridin-2-amine

생성물 1

HCID 582045954-Chloro-5-iodo-2-methoxypyridine수율 92.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 4-chloro-5-iodo-pyridin-2-ylamine (64.2 g, 0.25 mol) in methanol (1.1 L) and TFA (93.7 mL, 1.26 mol) was added tert-butyl nitrite (150 mL, 1.26 mol) so as to maintain temperature less than 3° C. The resultant mixture was stirred at RT for 1 h then allowed to warm to RT and stirred for 16 h. The reaction was quenched by the careful addition of water then concentrated in vacuo to ¼ volume. The resultant residue was treated with water (1 L) and the precipitate formed collected by filtration and dried in vacuo at 35° C. to give the title compound (62.3 g, 92%). Contains 16% impurity. 1H NMR 400 MHz (DMSO-d) δ: 8.56 (1 H, s), 7.20 (1 H, s), 3.86 (3 H, s).

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후처리

  1. temperatureto maintain temperature less than 3° C
  2. customThe reaction was quenched by the careful addition of water
  3. concentrationthen concentrated in vacuo
  4. additionThe resultant residue was treated with water (1 L)
  5. customthe precipitate formed
  6. filtrationcollected by filtration
  7. customdried in vacuo at 35° C.

출처 및 근거

ORD 기록
ord-0393a86864254fab83d50beae1a46b56
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09198918B2

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