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

Phosphorus sulfide (P2S5) → 1,3,4,5-Tetrahydro-2H-1-benzazepine-2-thione

HRID 80527
노트
인쇄 미리보기

반응식

HRID 80527 반응식
[NH:1]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH2:5][CH2:4][CH2:3][C:2]1=O.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:14]>N1C=CC=CC=1>[NH:1]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[CH2:5][CH2:4][CH2:3][C:2]1=[S:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14817Phosphorus sulfide (P2S5)HCID 2485801,3,4,5-Tetrahydro-2H-1-benzazepin-2-one

생성물 1

HCID 125454261,3,4,5-Tetrahydro-2H-1-benzazepine-2-thione

시약·촉매·용매 1

HCID 1049Pyridine용매

반응 조건

온도
120 °C

실험 절차

To a solution of Example 182A (12.435 g, 77 mmol) in pyridine (309 mL) under nitrogen was added phosphorus pentasulfide (34.3 g, 154 mmol), and the mixture was heated at 120° C. (reflux) for 2 hours. The solvent was decanted and water was added. The product was extracted with dichloromethane, pre-absorbed onto silica gel and purified by silica gel chromatography (Analogix IntelliFlash™ 280, SF10-150) eluting with 30% ethyl acetate/hexanes to obtain the title compound. 1H NMR (500 MHz, DMSO-d6) δ ppm 11.75 (s, 1H), 7.32-7.25 (m, 2H), 7.19 (td, J=7.5, 1.2, 1H), 7.10-7.00 (m, 1H), 2.63 (m, 4H), 2.20 (m, 2H); MS (ESI−) m/z 176.1 (M−H)−.

후처리

  1. temperature(reflux) for 2 hours
  2. customThe solvent was decanted
  3. additionwater was added
  4. extractionThe product was extracted with dichloromethane
  5. custompre-absorbed onto silica gel
  6. custompurified by silica gel chromatography (Analogix IntelliFlash™ 280, SF10-150)
  7. washeluting with 30% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-a22560ee744b479eba60d265586cf79a
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846663B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트