Dimethylformamide → HCID 67062125, 화합물

HRID 337554

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HRID 337554 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.CN(C=O)C.C(Cl)(=O)C(Cl)=O.[CH:23]1([NH2:26])[CH2:25][CH2:24]1.CCN(C(C)C)C(C)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([NH:26][CH:23]1[CH2:25][CH2:24]1)=[O:9]

참가 물질

7

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온도
0 °C

실험 절차

To a toluene solution (1 M) of 5-chloro-2-methylbenzoic acid (1 eq.) and DMF (1.2 eq.) was added at 0° C. oxalyl chloride (1.2 eq.) dropwise over 1 h. The resulting solution was stirred at 0° C. for 2 h before the volatiles were removed in vacuo. The resulting residue was taken up in dichloromethane (1 M), cooled to 0° C. and added sequentially cyclopropylamine (1.5 eq.) and Hunig's base (2 eq.) dropwise. The resulting suspension was stirred at RT for 18 h. The reaction was quenched with 1 N aq. HCl and extracted with dichloromethane. The combined organic extracts were dried over MgSO4, filtered and the filtrate concentrated in vacuo to ˜1/3 in volume. The resulting white suspension was added an equivalent volume of hexanes and the title compound was isolated via vacuum filtration.

후처리

  1. customwere removed in vacuo
  2. temperaturecooled to 0° C.
  3. stirringThe resulting suspension was stirred at RT for 18 h
  4. customThe reaction was quenched with 1 N aq. HCl
  5. extractionextracted with dichloromethane
  6. dry with materialThe combined organic extracts were dried over MgSO4
  7. filtrationfiltered
  8. concentrationthe filtrate concentrated in vacuo to ˜1/3 in volume
  9. additionThe resulting white suspension was added an equivalent volume of hexanes

출처 및 근거

ORD 기록
ord-4cb72e21895442acac8909515f40dfce
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08889714B2

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