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4-Methoxy-2-aminobenzothiazole → 2-Bromo-4-methoxy-1,3-benzothiazole

HRID 427286
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HRID 427286 반응식
N[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1.[Br-:13].[K+].N([O-])=O.[Na+]>S(=O)(=O)(O)O>[Br:13][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 216224-Methoxy-2-aminobenzothiazoleHCID 253877Potassium BromideHCID 23668193Sodium Nitrite

생성물 1

HCID 183569972-Bromo-4-methoxy-1,3-benzothiazole수율 78.8%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 2-amino-4-methoxybenzothiazole (1.5 g) and potassium bromide (3.5 g) in sulphuric acid (1.25M, 50 ml) at 0° C. was added sodium nitrite (0.86 g) over a period of 1 hr. The reaction was allowed to warm to room temperature and stirred for 2 hrs, before being extracted with dichloromethane (3×50 ml). The combined organic extracts were dried over magnesium sulphate (5 g), and the solvent removed in vacuo to yield an off white solid. This was purified by flash chromatography (eluent 50% ethyl acetate/hexane) to yield the title compound as a white solid (1.6 g). TLC Ff 0.30 (20% ethyl acetate in hexane)

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후처리

  1. extractionbefore being extracted with dichloromethane (3×50 ml)
  2. dry with materialThe combined organic extracts were dried over magnesium sulphate (5 g)
  3. customthe solvent removed in vacuo
  4. customto yield an off white solid
  5. customThis was purified by flash chromatography (eluent 50% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-d1caa672c92a4f6d8821d2f04995a1c3
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06313116B1

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