Diisopropylethylamine → Ethyl 8-bromo-6-chloro-7-(4-(6-(4-chlorophenyl)pyridin-2-ylcarbamoyl)phenoxy)chroman-4-carboxylate

HRID 1626459노트

반응식

HRID 1626459 반응식
[Br:1][C:2]1[C:3]([O:18][C:19]2[CH:27]=[CH:26][C:22]([C:23]([OH:25])=O)=[CH:21][CH:20]=2)=[C:4]([Cl:17])[CH:5]=[C:6]2[C:11]=1[O:10][CH2:9][CH2:8][CH:7]2[C:12]([O:14][CH2:15][CH3:16])=[O:13].Cl.[Cl:29][C:30]1[CH:35]=[CH:34][C:33]([C:36]2[N:41]=[C:40]([NH2:42])[CH:39]=[CH:38][CH:37]=2)=[CH:32][CH:31]=1.C(N(CC)C(C)C)(C)C>S(Cl)(Cl)=O.C(OCC)(=O)C.Cl>[Br:1][C:2]1[C:3]([O:18][C:19]2[CH:20]=[CH:21][C:22]([C:23](=[O:25])[NH:42][C:40]3[CH:39]=[CH:38][CH:37]=[C:36]([C:33]4[CH:34]=[CH:35][C:30]([Cl:29])=[CH:31][CH:32]=4)[N:41]=3)=[CH:26][CH:27]=2)=[C:4]([Cl:17])[CH:5]=[C:6]2[C:11]=1[O:10][CH2:9][CH2:8][CH:7]2[C:12]([O:14][CH2:15][CH3:16])=[O:13]

참가 물질

7

반응물 3

HCID 81531DiisopropylethylamineHCID 670804834-(8-Bromo-6-chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acidHCID 672887096-(4-Chlorophenyl)pyridin-2-amine hydrochloride

생성물 1

HCID 67287788Ethyl 8-bromo-6-chloro-7-(4-(6-(4-chlorophenyl)pyridin-2-ylcarbamoyl)phenoxy)chroman-4-carboxylate수율 58.4%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 8857Ethyl Acetate용매HCID 24386Thionyl Chloride용매

실험 절차

A solution of 4-(8-bromo-6-chloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acid (0.18 g, 0.40 mmol) in thionyl chloride (5 mL) was stirred and heated to gentle reflux for 30 minutes. The solution was cooled to ambient temperature and concentrated. The residual light yellow solid was dissolved in dichloromethane (4 mL). To the resulting stirred solution at ambient temperature was added 6-(4-chlorophenyl)pyridin-2-amine hydrochloride (96.6 mg, 0.40 mmol), followed by N,N-diisopropylethylamine (0.28 mL, 1.60 mmol). A solution formed, and stirring was continued at ambient temperature for 3 hours. The solution was diluted with ethyl acetate (20 mL) and 1M hydrochloric acid (10 mL), then transferred to a separatory funnel. After shaking, the organic layer was washed successively with 10 mL portions of water, 10% sodium carbonate, and brine, dried over sodium sulfate and evaporated. The residual oil was purified by chromatography on silica gel, eluting with 80/20 hexanes/ethyl acetate, to afford the desired compound as a colorless oil (0.15 g, 58% yield).

후처리

  1. temperatureheated
  2. temperatureto gentle reflux for 30 minutes
  3. concentrationconcentrated
  4. dissolutionThe residual light yellow solid was dissolved in dichloromethane (4 mL)
  5. customA solution formed
  6. stirringstirring
  7. customtransferred to a separatory funnel
  8. stirringAfter shaking
  9. washthe organic layer was washed successively with 10 mL portions of water, 10% sodium carbonate, and brine
  10. dry with materialdried over sodium sulfate
  11. customevaporated
  12. customThe residual oil was purified by chromatography on silica gel
  13. washeluting with 80/20 hexanes/ethyl acetate

출처 및 근거

ORD 기록
ord-f937d8121b764c35be6c47286dc3a066
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08785445B2

반응 노트

불러오는 중…