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

1,4-Dichlorobenzo[g]phthalazine → HCID 19699649, 화합물

HRID 862891
노트
인쇄 미리보기

반응식

HRID 862891 반응식
[Cl:1][C:2]1[C:11]2[CH:10]=[C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]3=[CH:7][C:6]=2[C:5](Cl)=[N:4][N:3]=1>C(N)CCC>[ClH:1].[CH2:2]([NH:3][C:2]1[C:11]2[CH:10]=[C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]3=[CH:7][C:6]=2[C:5]([NH:4][CH2:5][CH2:6][CH2:7][CH3:8])=[N:4][N:3]=1)[CH2:11][CH2:10][CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 153142771,4-Dichlorobenzo[g]phthalazine

생성물 1

HCID 19699649HCID 19699649, 화합물수율 112.9%

시약·촉매·용매 1

HCID 8007Butylamine용매

반응 조건

온도
130 °C

실험 절차

A mixture of 1,4-dichlorobenzo[g]phthalazine (9.23 mmol) and n-butylamine (20 mL) was heated in an autoclave at 130° C. for 12 h. After cooling to room temperature, the excess of n-butyl amine was evaporated to dryness under vacuum. When the residue was treated with acetone (100 mL) a yellow solid was formed. After being filtered off and dried it afforded 1.87 g (55% yield) of 1,4-bis(n-butylamino)benzo[g]phthalazine monohydrochloride. m.p. 195°-197° C.

후처리

  1. temperatureAfter cooling to room temperature
  2. customthe excess of n-butyl amine was evaporated to dryness under vacuum
  3. additionWhen the residue was treated with acetone (100 mL) a yellow solid
  4. customwas formed
  5. filtrationAfter being filtered off
  6. customdried it

출처 및 근거

ORD 기록
ord-22433bec48fb41509b1934ce986bd010
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05719282

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트