Formic Acid → HCID 178487492, 화합물

HRID 392580

반응식

HRID 392580 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([C:13]([C:15]1[N:16]=[CH:17][N:18](C(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)[CH:19]=1)=[O:14])[CH:7]=[CH:6]2.C(O)=O.[CH2:42]1[CH2:46]OC[CH2:43]1>>[NH:18]1[CH:19]=[C:15]([C:13]([C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH:4]=3)[CH:9]=2)([OH:14])[CH:42]([CH3:46])[CH3:43])[N:16]=[CH:17]1

참가 물질

4

반응물 3

HCID 284Formic AcidHCID 8028TetrahydrofuranHCID 11733735(6-Methoxynaphthalen-2-yl)-(1-trityl-1H-imidazol-4-yl)ketone

생성물 1

HCID 178487492HCID 178487492, 화합물

반응 조건

온도
50 °C

실험 절차

(6-Methoxynaphthalen-2-yl)-(1-trityl-1H-imidazol-4-yl)ketone (15.0 g) was dissolved in THF (80 ml) and 90% formic acid (20 ml) was added. The mixture was stirred at 50° C. for 2 h and the solvent was evaporated. 1N Hydrochloric acid (60 ml) was added and the precipitate was filtrated. The filtrate was washed with ether and neutralized with potassium carbonate. The resulting precipitate was collected by filtration and dried under reduced pressure to give the title compound (7.54 g) as a colorless solid.

후처리

  1. customthe solvent was evaporated
  2. addition1N Hydrochloric acid (60 ml) was added
  3. filtrationthe precipitate was filtrated
  4. washThe filtrate was washed with ether and neutralized with potassium carbonate
  5. filtrationThe resulting precipitate was collected by filtration
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-acd1013aaac349c5bb3de64a8bc69a98
출처 데이터셋
uspto-grants-2004_10
특허 번호
US06800778B1

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