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3-[3-(Dimethylamino)prop-2-enoyl]benzonitrile → 3-(2-Phenylamino-pyrimidin-4-yl)benzonitrile

HRID 968683
노트
인쇄 미리보기

반응식

HRID 968683 반응식
CN(C)[CH:3]=[CH:4][C:5]([C:7]1[CH:8]=[C:9]([CH:12]=[CH:13][CH:14]=1)[C:10]#[N:11])=O.[CH:16]1[CH:17]=[CH:18][C:19]([NH:22][C:23]([NH2:25])=[NH:24])=[CH:20][CH:21]=1>C(#N)C>[C:19]1([NH:22][C:23]2[N:25]=[C:5]([C:7]3[CH:8]=[C:9]([CH:12]=[CH:13][CH:14]=3)[C:10]#[N:11])[CH:4]=[CH:3][N:24]=2)[CH:20]=[CH:21][CH:16]=[CH:17][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 28062053-[3-(Dimethylamino)prop-2-enoyl]benzonitrileHCID 178418923HCID 178418923, 화합물

생성물 1

HCID 671143483-(2-Phenylamino-pyrimidin-4-yl)benzonitrile

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

To a solution of 3-(3-dimethylamino-acryloyl)-benzonitrile (30.4 g, 152 mmol) in acetonitrile (250 mL) was added a solution of phenylguanidine (21.0 g, 155 mmol) in acetonitrile (250 mL) and the mixture was heated at reflux for two hours. The solution was cooled and the resulting solid was filtered and washed with acetonitrile to afford the title compound.

후처리

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  1. temperaturethe mixture was heated
  2. temperatureat reflux for two hours
  3. temperatureThe solution was cooled
  4. filtrationthe resulting solid was filtered
  5. washwashed with acetonitrile

출처 및 근거

ORD 기록
ord-2bbc592dfc1f41849c253becfbfb3038
출처 데이터셋
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07304071B2

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