Dichloromethane → HCID 67190457, 화합물

HRID 551821노트

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HRID 551821 반응식
[N:1]1([C:11]2[CH:19]=[CH:18][C:14]([C:15]([OH:17])=[O:16])=[C:13]([O:20][CH3:21])[CH:12]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4][CH2:3][CH2:2]1.Cl[CH2:23]Cl.ClC(Cl)(O[C:29](=[O:35])OC(Cl)(Cl)Cl)Cl.Cl.Cl.[NH:39]1[CH2:43][CH2:42][CH:41]([C:44]2[CH:45]=[N:46][NH:47][CH:48]=2)[CH2:40]1>C(N(CC)CC)C>[CH3:23][O:16][C:15](=[O:17])[C:14]1[CH:18]=[CH:19][C:11]([N:1]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[N:4]([C:29]([N:39]3[CH2:43][CH2:42][CH:41]([C:44]4[CH:45]=[N:46][NH:47][CH:48]=4)[CH2:40]3)=[O:35])[CH2:3][CH2:2]2)=[CH:12][C:13]=1[O:20][CH3:21]

참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 94429TriphosgeneHCID 67186545HCID 67186545, 화합물HCID 671872294-(pyrrolidin-3-yl)-1H-pyrazole dihydrochloride

생성물 1

HCID 67190457HCID 67190457, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

0.92 g of the methyl ester of 4-(3,4-dihydro-2H-quinoxalin-1-yl)-2-methoxybenzoic acid and 15 ml of dichloromethane are introduced into a three-necked flask equipped with a magnetic stirrer and placed under an inert atmosphere. After cooling to +4° C., 1.92 ml of triethylamine and 0.33 g of triphosgene are successively added. The reaction medium is stirred at ambient temperature for 3 h. 0.64 g of 4-pyrrolidin-3-yl-1H-pyrazole dihydrochloride is then introduced and the mixture is stirred at ambient temperature for 18 h. The reaction medium is washed with a saturated aqueous sodium hydrogencarbonate solution; the organic phase is dried over sodium sulfate and concentrated under reduced pressure. The residue is chromatographed on silica gel eluted with a gradient of methanol from 2% to 4% in dichloromethane. The product obtained is rechromatographed on silica gel eluted with a dichloromethane/methanol 99/1 to 92/8 gradient. 1.06 g of 2-methoxy-4-{4-[3-(1H-pyrazol-4-yl)pyrrolidine-1-carbonyl]-3,4-dihydro-2H-quinoxalin-1-yl}benzoic acid methyl ester are obtained.

후처리

  1. customequipped with a magnetic stirrer
  2. temperatureAfter cooling to +4° C.
  3. stirringthe mixture is stirred at ambient temperature for 18 h
  4. washThe reaction medium is washed with a saturated aqueous sodium hydrogencarbonate solution
  5. dry with materialthe organic phase is dried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue is chromatographed on silica gel
  8. washeluted with a gradient of methanol from 2% to 4% in dichloromethane
  9. customThe product obtained
  10. customis rechromatographed on silica gel
  11. washeluted with a dichloromethane/methanol 99/1 to 92/8 gradient

출처 및 근거

ORD 기록
ord-8f291cb43f7240bda6e390a8453cf1cf
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07947834B2

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