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

Ammonia → 4-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

HRID 2392866
노트
인쇄 미리보기

반응식

HRID 2392866 반응식
[NH3:1].C([O:4][C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)=O)C>C(O)C>[C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)(=[O:4])[NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 18796707HCID 18796707, 화합물

생성물 1

HCID 187967044-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

20 ml of a 10% solution of ammonia in ethanol was added to 200 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was stirred at room temperature for 3 days. The crystal thus precipitated was recovered by filtration. Thus, 60 mg of the title compound was obtained.

후처리

  1. custom
The crystal thus precipitated
  • filtrationwas recovered by filtration
  • 출처 및 근거

    ORD 기록
    ord-2e6aac06acb845ab9c63e207a32f4fde
    출처 데이터셋
    uspto-grants-1998_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05801180

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트