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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 15516970, 화합물

HRID 1250304
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HRID 1250304 반응식
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:14]2[N:19]=[CH:18][CH:17]=[CH:16][N:15]=2)=[CH:10][CH2:9]1)=O)(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[N:15]1[CH:16]=[CH:17][CH:18]=[N:19][C:14]=1[C:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acid2회HCID 18327906HCID 18327906, 화합물

생성물 1

HCID 15516970HCID 15516970, 화합물수율 87%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

500 mg of the compound of step 2 of Example 25 was dissolved in 10 ml of methylene chloride, 3.5 ml of trifluoroacetic acid (hereinafter referred to as TFA) was added, then the resultant mixture was agitated at room temperature for 30 minutes. This was concentrated, then an aqueous solution of 10% sodium hydroxide was added and extraction was performed with chloroform. The organic layer was washed by saturated saline and was dried with anhydrous magnesium sulfate. This chloroform was concentrated to obtain the above-referenced compound in an amount of 260 mg (yield of 87%).

후처리

  1. additionwas added
  2. concentrationThis was concentrated
  3. additionan aqueous solution of 10% sodium hydroxide was added
  4. extractionextraction
  5. washThe organic layer was washed by saturated saline
  6. dry with materialwas dried with anhydrous magnesium sulfate
  7. concentrationThis chloroform was concentrated
  8. customto obtain the above-referenced compound in an amount of 260 mg (yield of 87%)

출처 및 근거

ORD 기록
ord-113e3b6269224ed7a9aada12acbe05c7
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06337397B1

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