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Triethylamine → 1-(3-chloro-4-methoxyphenyl)-N-(6'-methoxy-3,5'-dimethyl-2,3'-bipyridin-6-yl)cyclopropanecarboxamide

HRID 870008
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HRID 870008 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2([C:13]([OH:15])=O)[CH2:12][CH2:11]2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].S(Cl)(Cl)=O.[CH3:20][O:21][C:22]1[N:27]=[CH:26][C:25]([C:28]2[C:33]([CH3:34])=[CH:32][CH:31]=[C:30]([NH2:35])[N:29]=2)=[CH:24][C:23]=1[CH3:36].CCN(CC)CC>ClCCl.CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2([C:13]([NH:35][C:30]3[N:29]=[C:28]([C:25]4[CH:26]=[N:27][C:22]([O:21][CH3:20])=[C:23]([CH3:36])[CH:24]=4)[C:33]([CH3:34])=[CH:32][CH:31]=3)=[O:15])[CH2:11][CH2:12]2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]
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참가 물질

7

반응물 4

HCID 8471TriethylamineHCID 24386Thionyl ChlorideHCID 591294641-(3-Chloro-4-methoxyphenyl)cyclopropane-1-carboxylic acidHCID 68722468HCID 68722468, 화합물

생성물 1

HCID 687245221-(3-chloro-4-methoxyphenyl)-N-(6'-methoxy-3,5'-dimethyl-2,3'-bipyridin-6-yl)cyclopropanecarboxamide수율 50.2%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
촉매
HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 1-(3-chloro-4-methoxyphenyl)cyclopropanecarboxylic acid (45.3 mg, 0.2 mmol) in dichloromethane (2 mL) was added thionyl chloride (43.8 μL, 0.60 mmol) followed by DMF (1 drop) and the reaction was stirred at room temperature for 30 minutes and then the solvent was evaporated. Toluene (˜1 mL) was added and mixed with the residue and then evaporated. The residue was then dissolved in dichloromethane (1 mL) and a solution of 6′-methoxy-3,5′-dimethyl-2,3′-bipyridin-6-amine (45.9 mg, 0.20 mmol) and Et3N (83.6 μL, 0.60 mmol) in dichloromethane (1 mL) was added. The reaction was stirred at room temperature for 12 hours and then the reaction was then concentrated. The residue was dissolved in DMSO and purified by HPLC (10-99% acetonitrilein water) to yield 44 mg of the product. ESI-MS m/z calc. 437.1. found 438.1 (M+1)+. Retention time 2.10 minutes.

후처리

  1. customthe solvent was evaporated
  2. additionToluene (˜1 mL) was added
  3. additionmixed with the residue
  4. customevaporated
  5. dissolutionThe residue was then dissolved in dichloromethane (1 mL)
  6. stirringThe reaction was stirred at room temperature for 12 hours
  7. concentrationthe reaction was then concentrated
  8. dissolutionThe residue was dissolved in DMSO
  9. custompurified by HPLC (10-99% acetonitrilein water)

출처 및 근거

ORD 기록
ord-cd9cd6bf06cd4aceb1d5d3ea73ef9972
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969386B2

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