Phosphorus oxychloride → HCID 53486023, 화합물

HRID 470323노트

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HRID 470323 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:15]3[N:14]=[C:13](O)[N:12]=[CH:11][C:10]=3[CH2:9][CH2:8][C:7]=2[CH:17]=1.N1C2C3C=CC=CC=3CCC=2C=NC=1O.O=P(Cl)(Cl)[Cl:35]>>[Cl:35][C:13]1[N:12]=[CH:11][C:10]2[CH2:9][CH2:8][C:7]3[CH:17]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=3[C:15]=2[N:14]=1

참가 물질

4

반응물 3

HCID 24813Phosphorus oxychlorideHCID 178487123HCID 178487123, 화합물HCID 1785175485,6-Dihydrobenzo[h]quinazolin-2-ol

생성물 1

HCID 53486023HCID 53486023, 화합물수율 86%

반응 조건

온도
100 °C

실험 절차

A suspension of 8-Methoxy-5,6-dihydro-benzo[h]quinazolin-2-ol as a 1:1 urea complex from preparation 1 (20 g, 69.0 mM) in POCl3 (350 ml) was heated under nitrogen atmosphere at 100° C. for 20 hr. The POCl3 was removed under reduced pressure and the residue was suspended in dichloromethane (300 ml) and cooled in an ice bath and then concentrated sodium bicarbonate (500 ml) was carefully added followed by 1 N NaOH (200 ml) and the phases separated. The aqueous phase was extracted with dichloromethane (3×500 ml) and the pooled organic phases were dried over Na2SO4, filtered and the filtrate evaporated under reduced pressure to give 2-Chloro-8-methoxy-5,6-dihydro-benzo[h]quinazoline (2, 14.46 g, 86% yield) as a yellow solid. ES-MS MH+ 247.1. 1H NMR (300 MHz, ppm, DMSO-d6): 8.54 (s, 1H), 8.09 (d, 1H), 6.99 (m, 3H) 3.84 (s, 3H), 2.91 (m, 4H).

후처리

  1. customThe POCl3 was removed under reduced pressure
  2. temperaturecooled in an ice bath
  3. additionconcentrated sodium bicarbonate (500 ml) was carefully added
  4. customthe phases separated
  5. extractionThe aqueous phase was extracted with dichloromethane (3×500 ml)
  6. dry with materialthe pooled organic phases were dried over Na2SO4
  7. filtrationfiltered
  8. customthe filtrate evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-531113abc9c748c99e32a93996247292
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08629147B2

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