1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) → HCID 178428840, 화합물

HRID 2415463노트

반응식

HRID 2415463 반응식
C(O[C:4](=[O:23])[CH:5]=[C:6]([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:10]=1)[CH3:7])C.C1C=CC(C2C=CC=CC=2)=CC=1.C1C=CC(OC2C=CC=CC=2)=CC=1>CCCCCCC>[CH2:16]([O:15][C:11]1[CH:10]=[C:9]2[C:14]([C:4]([OH:23])=[CH:5][C:6]([CH3:7])=[N:8]2)=[CH:13][CH:12]=1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

참가 물질

4

반응 조건

온도
250 °C

실험 절차

3.67 g (11.8 mmol) of 3-(3-benzyloxy-phenylamino)-but-2-enoic acid ethyl ester were added dropwise within 20 minutes to 5.5 ml of Dowtherm A heated at 250° C. (metal bath temperature). The solution was stirred further 10 minutes at 250° C. (bath temperature), cooled to RT and then treated with 20 ml of heptane. The brown viscous oil that had formed was isolated and triturated with 45 ml of AcOEt. The brown solid obtained was filtered off by suction, washed with AcOEt and dried in a high vacuum to give 1.19 g (35%) of 7-benzyloxy-2-methyl-quinolin-4-ol. ISP mass spectrum, m/e: 266.3 (M+1 calculated for C17H15NO2: 266).

후처리

  1. temperaturecooled to RT
  2. customThe brown viscous oil that had formed
  3. customwas isolated
  4. customtriturated with 45 ml of AcOEt
  5. customThe brown solid obtained
  6. filtrationwas filtered off by suction
  7. washwashed with AcOEt
  8. customdried in a high vacuum

출처 및 근거

ORD 기록
ord-58c35639ed31437e95741d42c38739c3
출처 데이터셋
uspto-grants-2004_11
특허 번호
US06818767B2

반응 노트

불러오는 중…