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Potassium Carbonate → 5-Bromo-6-methoxybenzo[d]isoxazol-3-ylamine

HRID 2396726
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HRID 2396726 반응식
[NH2:1][C:2]1[C:6]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N:3]=1.[Br:13]Br.C([O-])([O-])=O.[K+].[K+].[O-]S([O-])=O.[Na+].[Na+]>CO.CC(C)=O.C(Cl)(Cl)Cl>[NH2:1][C:2]1[C:6]2[CH:7]=[C:8]([Br:13])[C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 11430Potassium CarbonateHCID 24408Bromine2회HCID 24437Sodium SulfiteHCID 106785796-Methoxy-1,2-benzoxazol-3-amine

생성물 1

HCID 187964575-Bromo-6-methoxybenzo[d]isoxazol-3-ylamine수율 67.7%

시약·촉매·용매 2

HCID 887Methanol
용매
2회
HCID 15930782Chloroform acetone용매

실험 절차

To a stirred solution of 3-amino-6-methoxy-1,2-benzisoxazole (14 g) in methanol (1 L) was added a solution of bromine (13.6 g) and methanol (200 ml) dropwise at -50° C. under N2. The mixture was allowed to warm to room temperature after the addition was complete. After 24 hours an additional 1/4 equivalent of bromine was added. TLC (10% acetone/CHCl3) showed no starting material 24 hours later. The reaction was neutralized with saturated K2CO3 solution, treated with saturated Na2SO3 solution triturated with water, filtered, and washed with water. The crude product was dried in vacuo affording 14 g of product, m.p. 226°-227° C.

후처리

  1. additionafter the addition
  2. customno starting material 24 hours
  3. customtriturated with water
  4. filtrationfiltered
  5. washwashed with water
  6. dry with materialThe crude product was dried in vacuo

출처 및 근거

ORD 기록
ord-c5b55bef8ab349fc9ad59fb32009f32e
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05494908

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