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Ammonia → HCID 86643508, 화합물

HRID 1968620
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인쇄 미리보기

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HRID 1968620 반응식
[CH2:1]([N:3]([C:10]1[CH:19]=[CH:18][CH:17]=[C:16]2[C:11]=1[CH:12]=[CH:13][CH:14]=[C:15]2[S:20](Cl)(=[O:22])=[O:21])[C:4](=[O:9])[C:5]([F:8])([F:7])[F:6])[CH3:2].[NH3:24]>O1CCCC1>[CH2:1]([N:3]([C:10]1[C:11]2[C:16](=[C:15]([S:20](=[O:22])(=[O:21])[NH2:24])[CH:14]=[CH:13][CH:12]=2)[CH:17]=[CH:18][CH:19]=1)[C:4](=[O:9])[C:5]([F:8])([F:7])[F:6])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 2758932HCID 2758932, 화합물

생성물 1

HCID 86643508HCID 86643508, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

5-(N-ethyl-2,2,2-trifluoroacetamido)naphthalene-1-sulfonyl chloride (100 mg) was dissolved in tetrahydrofuran (1.0 mL), cooled to 0° C., then concentrated ammonia (0.11 mL) was added. The reaction was stirred at 0° C. for 3 hours, then concentrated and partitioned between water and ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated to give the title compound.

후처리

  1. concentrationconcentrated
  2. custompartitioned between water and ethyl acetate
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-27ffeb68260443e085a5d580011c55a5
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426422B2

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