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Hydrochloric Acid → HCID 57439914, 화합물

HRID 906455
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인쇄 미리보기

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HRID 906455 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[NH:7][CH:6]=[C:5]2[S:13](Cl)(=O)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O.Cl>C1COCC1.C(OCC)(=O)C.CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=[O:12])[NH:7][CH:6]=[C:5]2[SH:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 11776TriphenylphosphineHCID 574399006-Bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chloride

생성물 1

HCID 57439914HCID 57439914, 화합물수율 25.2%

시약·촉매·용매 3

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 6-bromo-1-oxo-1,2-dihydroisoquinoline-4-sulfonyl chloride (Example 46a, 1 g) in THF (12 mL) was added triphenylphosphine (2.85 g). After 5 min, water (0.48 mL) was added followed by DMF (0.6 mL) and the reaction stirred for 1 h. Ethyl acetate and 2M HCl (aq) were added and the mixture shaken vigorously. The solid was filtered off and washed with further water and ethyl acetate before drying in vacuo at room temperature is for 2 h to afford the subtitle compound (0.2 g).

후처리

  1. stirringthe mixture shaken vigorously
  2. filtrationThe solid was filtered off
  3. washwashed with further water and ethyl acetate
  4. custombefore drying in vacuo at room temperature
  5. waitis for 2 h

출처 및 근거

ORD 기록
ord-fd6392823a4747a2bef17464c98e432a
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012980B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매