홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Pyridine → HCID 21494726, 화합물

HRID 1731101
노트
인쇄 미리보기

반응식

HRID 1731101 반응식
[NH2:1][N:2]1[C:11]([OH:18])([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([Cl:19])[CH:9]=2)[N:4]=[CH:3]1.N1C=CC=CC=1.[C:26]1(=[O:41])[N:30]([CH2:31][CH2:32][C:33](Cl)=O)[C:29](=[O:36])[C:28]2=[CH:37][CH:38]=[CH:39][CH:40]=[C:27]12.C(=O)(O)[O-].[Na+]>O1CCCC1>[Cl:19][C:8]1[CH:7]=[CH:6][C:5]([N:4]2[CH:3]=[N:2][N:1]=[C:33]2[CH2:32][CH2:31][N:30]2[C:29](=[O:36])[C:28]3=[CH:37][CH:38]=[CH:39][CH:40]=[C:27]3[C:26]2=[O:41])=[C:10]([CH:9]=1)[C:11]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 869661,3-dihydro-1,3-dioxo-2H-isoindole-2-propionyl chlorideHCID 1196793-Amino-6-chloro-3,4-dihydro-4-phenylquinazolin-4-olHCID 516892Sodium Bicarbonate

생성물 1

HCID 21494726HCID 21494726, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매
2회

실험 절차

A stirred mixture of 3-amino-6-chloro-3,4-dihydro-4-hydroxy-4-phenylquinazoline (2.74 g. 0.01 mole) in dry tetrahydrofuran (150 ml.) is cooled in an ice bath, under nitrogen, and treated with dry pyridine (1.77 ml., 0.022 mole). This mixture is then treated dropwise, during 1 hour with a solution of β-phthalimidopropionyl chloride (5.23 g., 0.022 mole) in tetrahydrofuran (25 ml.). The mixture is kept in the ice bath for 1 hour and at ambient temperature for 4 hours. It is then poured into cold, dilute aqueous sodium bicarbonate and extracted with chloroform. The extract is washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue is mixed with toluene (165 ml.), treated with trifluoroacetic acid (0.732 ml.) and warmed, under nitrogen at 100°-110° C. for 1.5 hours. The mixture is concentrated in vacuo and the residue mixed with cold water and extracted with chloroform. The extract is washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue is chromatographed on silica gel (300 g) with 1.5% methanol-98.5% chloroform. The product thus obtained is crystallized to give 5-chloro-2-[3-(2-phthalimidoethyl)-4H-1,2,4-triazol-4-yl]benzophenone.

후처리

  1. temperatureis cooled in an ice bath, under nitrogen
  2. extractionextracted with chloroform
  3. washThe extract is washed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. additionThe residue is mixed with toluene (165 ml.)
  7. additiontreated with trifluoroacetic acid (0.732 ml.)
  8. temperaturewarmed, under nitrogen at 100°-110° C. for 1.5 hours
  9. concentrationThe mixture is concentrated in vacuo
  10. additionthe residue mixed with cold water
  11. extractionextracted with chloroform
  12. washThe extract is washed with brine
  13. dry with materialdried over anhydrous sodium sulfate
  14. concentrationconcentrated
  15. customThe residue is chromatographed on silica gel (300 g) with 1.5% methanol-98.5% chloroform
  16. customThe product thus obtained
  17. customis crystallized

출처 및 근거

ORD 기록
ord-f9b994b2990346ad914649f5670b8862
출처 데이터셋
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03994940

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트