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

Potassium Bromide → 6-Amino-2-(2,3-dihydro-1,4-benzodioxin-6-yl)-quinazoline

HRID 1670683
노트
인쇄 미리보기

반응식

HRID 1670683 반응식
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]1[CH:17]=[CH:16][C:15]3[O:18][CH2:19][O:20][C:14]=3[CH:13]=1)[N:6]=[CH:5]2.[K+].[Br-].[CH:23](Cl)(Cl)Cl.CO>>[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]1[CH:17]=[CH:16][C:15]3[O:18][CH2:23][CH2:19][O:20][C:14]=3[CH:13]=1)[N:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 253877Potassium BromideHCID 21584188Chloroform methanolHCID 441404276-Amino-2-(3,4-methylendioxy-phenyl)quinazoline

생성물 1

HCID 578631656-Amino-2-(2,3-dihydro-1,4-benzodioxin-6-yl)-quinazoline수율 67%

실험 절차

This compound was synthesized in 67% yield, according to the procedure described in example 3 for 6-amino-2-(3,4-methylendioxy-phenyl)-quinazoline. C16H13N3O2, MW: 279.30. mp 179.4-181.6° C.; 1H NMR (DMSO-d6) 9.24 (s, 1H), 7.92-7.98 (m, 2H), 7.72 (d, 1H), 7.38 (dd, 1H), 6.89-6.99 (m, 2H), 5.91 (s, 2H), 4.31 (s, 4H); IR (KBr) 1555, 1507, 1286; TLC (CHCl3/MeOH 9/1) Rf=0.65.

후처리

  1. customThis compound was synthesized in 67% yield

출처 및 근거

ORD 기록
ord-fc09ee218fe84956a7d2ef09eb73d48a
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994181B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트