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P-Anisidine → 7-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

HRID 30984
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HRID 30984 반응식
Cl[S:2]([N:5]=[C:6]=[O:7])(=[O:4])=[O:3].[CH3:8][O:9][C:10]1[CH:16]=[CH:15][C:13]([NH2:14])=[CH:12][CH:11]=1.[Cl-].[Al+3].[Cl-].[Cl-]>[N+](CC)([O-])=O>[CH3:8][O:9][C:10]1[CH:16]=[CH:15][C:13]2[NH:14][C:6](=[O:7])[NH:5][S:2](=[O:4])(=[O:3])[C:12]=2[CH:11]=1
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참가 물질

5

반응물 3

HCID 7732P-AnisidineHCID 70918Chlorosulfonyl isocyanateHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 125284907-Methoxy-2H-benzo[e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide수율 95%

시약·촉매·용매 1

HCID 6587Nitroethane용매2회

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온도
-40 °C

실험 절차

A solution of chlorosulfonyl isocyanate (17 mL, 195 mmol.) was dissolved in 150 mL of nitroethane and cooled to −40° C. A solution of 4-methoxyaniline (Z) (20 g, 162 mmol) in 100 mL of nitroethane was then added drop-wise from a dropper funnel with stirring. After the addition was completed, the reaction was stirred for an additional 5 minutes and aluminum chloride (25 g, 195 mmol) was added. The mixture was then quickly heated to 110° C. with stirring for 20 minutes. The crude material was then poured onto ice and the precipitate was collected by suction filtration, washed with cold water, and dried in vacuo to produce 35 g of the desired product (8) as a purple powder in 95% yield. 1H NMR (400 MHz, DMSO-d6): δ 11.05 (s, 1H), 7.2 (m, 3H), 3.78 (s, 3H), 3.6 (br, 1H).

후처리

  1. additionAfter the addition
  2. stirringthe reaction was stirred for an additional 5 minutes
  3. temperatureThe mixture was then quickly heated to 110° C.
  4. stirringwith stirring for 20 minutes
  5. filtrationthe precipitate was collected by suction filtration
  6. washwashed with cold water
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-6983da0e423f4f0586daf65b5c99150f
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07425552B2

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