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Hydrochloric Acid → HCID 19083159, 화합물

HRID 1378934
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HRID 1378934 반응식
CN(C)C=[N:4][S:5]([C:8]1[N:9]([CH3:21])[N:10]=[C:11]2[C:16]=1[C:15]([O:17][CH2:18][CH2:19][F:20])=[CH:14][CH:13]=[CH:12]2)(=[O:7])=[O:6].Cl>C(O)C>[F:20][CH2:19][CH2:18][O:17][C:15]1[C:16]2[C:11]([CH:12]=[CH:13][CH:14]=1)=[N:10][N:9]([CH3:21])[C:8]=2[S:5]([NH2:4])(=[O:6])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86749619N1,N1-dimethyl-N2-([4-(2-fluoroethoxy)-2-methyl-2H-indazol-3-yl]sulfonyl}formamidine

생성물 1

HCID 19083159HCID 19083159, 화합물수율 85%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture comprising 3.4 g of N1,N1 -dimethyl-N2 -{[4-(2-fluoroethoxy)-2-methyl-2H-indazol-3-yl]sulfonyl}formamidine, 5 ml of concentrated hydrochloric acid and 50 ml of ethanol, was refluxed for 12 hours. Disappearance of the starting material was confirmed by TLC, and then ethanol was distilled off. Water was added to the residue, whereupon the formed crystals were collected by filtration and washed with water and IPE to obtain 2.4 g (yield: 85%) of the desired product. Melting point: 178°-180° C.

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후처리

  1. temperaturewas refluxed for 12 hours
  2. distillationethanol was distilled off
  3. additionWater was added to the residue, whereupon the formed crystals
  4. filtrationwere collected by filtration
  5. washwashed with water and IPE

출처 및 근거

ORD 기록
ord-ef0aba797360410bae35aa3fe2b6524c
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670452

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