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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 66759651, 화합물

HRID 389479
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HRID 389479 반응식
[Br:1][C:2]1[C:10]2[S:9][CH:8]=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1N.Cl.N([O-])=O.[Na+].[I-:17].[K+].S([O-])([O-])(=O)=S.[Na+].[Na+]>O>[Br:1][C:2]1[C:10]2[S:9][CH:8]=[N:7][C:6]=2[CH:5]=[CH:4][C:3]=1[I:17]
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참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 4875Potassium IodideHCID 24477Sodium ThiosulfateHCID 47126206-Amino-7-bromobenzothiazoleHCID 23668193Sodium Nitrite

생성물 1

HCID 66759651HCID 66759651, 화합물수율 5%

시약·촉매·용매 1

HCID 962
Water
용매
4회

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온도
0 °C

실험 절차

To a suspension of 7-bromo-benzothiazol-6-ylamine (7.6 g, 33.3 mmol) in water (60 mL) was added concentrated hydrochloric acid (6 mL, 72 mmol). The mixture was cooled to 0° C. and stirred for 10 min. A cooled (0° C.) solution of sodium nitrite (5.0 g, 73 mmol) in water (10 mL) was added dropwise to the reaction mixture keeping the internal temperature below 5° C. The mixture was stirred for further 10 min. A solution of potassium iodide (12.1 g, 73 mmol) in water (15 mL) was added to the reaction mixture and was stirred vigorously for 10 min, and then water (200 mL) and 20% aqueous sodium thiosulfate solution (100 mL) were added. The solid formed was extracted with ethyl acetate (3×70 mL). The combined organic fractions were washed with water (100 mL), dried over anhydrous sodium sulfate, and concentrated. Purification of the residue by column chromatography (25% ethyl acetate:hexanes) afforded 0.3 g (5%) of the title compound, plus some impure title compound. The impure title compound was recrystallized 2× from 1:4 DCM:hexanes to afford a further 0.71 g (9%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 8.99 (s, 1H), 7.95 (d, J=8.4, 1H), 7.77 (d, J=8.4 Hz, 1H).

후처리

  1. additionwas added dropwise to the reaction mixture
  2. customthe internal temperature below 5° C
  3. stirringThe mixture was stirred for further 10 min
  4. stirringwas stirred vigorously for 10 min
  5. customThe solid formed
  6. extractionwas extracted with ethyl acetate (3×70 mL)
  7. washThe combined organic fractions were washed with water (100 mL)
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated
  10. customPurification of the residue by column chromatography (25% ethyl acetate:hexanes)

출처 및 근거

ORD 기록
ord-c0b285f54991407c8be56ed931932c99
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378104B2

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