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Guaiacol → HCID 22054602, 화합물

HRID 1006142
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HRID 1006142 반응식
CC(OC(/N=N/C(OC(C)C)=O)=O)C.Cl[C:16]1[C:25]2[C:20](=[CH:21][C:22]([CH2:26][OH:27])=[CH:23][CH:24]=2)[N:19]=[C:18]([CH3:28])[CH:17]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1O.[NH:57]1[CH2:61][CH2:60][CH2:59][CH2:58]1.[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64]>ClCCl.C(O)C>[C:62]([OH:67])(=[O:66])[C:63]([OH:65])=[O:64].[CH3:48][O:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][C:51]=1[O:27][CH2:26][C:22]1[CH:21]=[C:20]2[C:25]([C:16]([N:57]3[CH2:61][CH2:60][CH2:59][CH2:58]3)=[CH:17][C:18]([CH3:28])=[N:19]2)=[CH:24][CH:23]=1
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참가 물질

9

반응물 6

HCID 460GuaiacolHCID 971Oxalic AcidHCID 11776TriphenylphosphineHCID 31268PyrrolidineHCID 5363146Diisopropyl azodicarboxylateHCID 11264243HCID 11264243, 화합물

생성물 1

HCID 22054602HCID 22054602, 화합물
수율 43%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매

실험 절차

Diisopropylazodicarboxylate (97 mg, 0.48 mmol) was added dropwise at r.t. to a solution of (4-chloro-2-methyl-quinolin-7-yl)-methanol (example 2c, 100 mg, 0.48 mmol), triphenylphosphine (126 mg, 0.48 mmol), 2-methoxyphenol (60 mg, 0.48 mmol) in dichloromethane (2.5 mL). After shaking 24 h at r.t., the solvent was evaporated, and the residue was taken up in pyrrolidine (1.37 g, 19.2 mmol) and shaken for 23 h at 80° C. After cooling the reaction mixture was partitioned between sat. aq. ammonium chloride solution and dichloromethane, the organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which was dissolved in ethanol and treated with 20% ethanolic oxalic acid solution. The precipitate was collected by filtration and dried to afford the title compound (90 mg, 43%). Off-white solid, ISP-MS: m/e=349.4 ([M+H—C2H2O4]+).

후처리

  1. customthe solvent was evaporated
  2. stirringshaken for 23 h at 80° C
  3. temperatureAfter cooling the reaction mixture
  4. customwas partitioned between sat. aq. ammonium chloride solution and dichloromethane
  5. washthe organic layer was washed with brine
  6. dry with materialdried (MgSO4)
  7. customevaporated
  8. customChromatography (SiO2, dichloromethane/methanol 19:1) yielded a yellowish solid which
  9. filtrationThe precipitate was collected by filtration
  10. customdried

출처 및 근거

ORD 기록
ord-3460d1419998418fbea719f32b1273b2
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06787558B2

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