반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]3[CH:15]=[C:14]([O:16][CH2:17][CH2:18][Cl:19])[C:13]([O:20][CH3:21])=[CH:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:22]#[N:23].ClC1C2C(=CC3C=C(OC)C(OCCCl)=CC=3C=2)N=CC=1C#N.Cl.N1C=CC=CC=1.[Cl:54][C:55]1[CH:61]=[C:60]([Cl:62])[C:59]([O:63][CH3:64])=[CH:58][C:56]=1[NH2:57].C(OCCO)C>>[Cl:54][C:55]1[CH:61]=[C:60]([Cl:62])[C:59]([O:63][CH3:64])=[CH:58][C:56]=1[NH:57][C:2]1[C:11]2[C:6](=[CH:7][C:8]3[CH:15]=[C:14]([O:16][CH2:17][CH2:18][Cl:19])[C:13]([O:20][CH3:21])=[CH:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:22]#[N:23]참가 물질
반응물 5
생성물 1
반응 조건
- 온도
- 135 °C
실험 절차
A mixture of 1.10 g (3.17 mmol) of 4-chloro-7-methoxy-8-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile and 4-chloro-8-methoxy-7-(2-chloroethoxy)benzo[g]quinoline-3-carbonitrile (1:1 mixture), 50 mg of pyridine hydrochloride, 742 mg (3.86 mmol) of 2,4-dichloro-5-methoxyaniline and 25 mL of 2-ethoxyethanol is stirred and heated to 135° C. After 1 hour, the reaction is cooled to room temperature, quenched with 1.0 mL of triethylamine and concentrated in vacuo. The residue is dissolved in 95:5 methylene chloride/methanol and chromatographed on silica gel, eluting with 1:1 hexane/ethyl acetate. The product is precipitated from ethyl acetate to provide 0.760 g (48%) of 4-(2,4-dichloro-5-methoxyanilino)-7-methoxy-8-(chloroethoxy)benzo[g]quinoline-3-carbonitrile and 4-(2,4-dichloro-5-methoxyanilino)-8-methoxy-7(chloroethoxy)benzo[g]quinoline-3-carbonitrile (1:1 mixture) as a dull yellow solid, m.p. 239-55° C. dec.
후처리
- temperaturethe reaction is cooled to room temperature
- customquenched with 1.0 mL of triethylamine
- concentrationconcentrated in vacuo
- dissolutionThe residue is dissolved in 95:5 methylene chloride/methanol
- customchromatographed on silica gel
- washeluting with 1:1 hexane/ethyl acetate
- customThe product is precipitated from ethyl acetate
출처 및 근거
- ORD 기록
- ord-74b21ec7a4f74e91a6bed0248c332ccb
- 출처 데이터셋
- uspto-grants-2003_10
- 특허 번호
- US06638929B2
연결된 노트
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