Acetic Acid → HCID 23113351, 화합물

HRID 75509

반응식

HRID 75509 반응식
[C:1](O)(=O)C.[Cl:5][C:6]1[CH:11]=[C:10](OC)[CH:9]=[CH:8][C:7]=1[CH:14]([C:17](=O)[CH3:18])[C:15]#[N:16].[OH2:20].[NH2:21][NH2:22]>C1(C)C=CC=CC=1>[Cl:5][C:6]1[CH:11]=[C:10]([O:20][CH3:1])[CH:9]=[CH:8][C:7]=1[C:14]1[C:15]([NH2:16])=[N:21][NH:22][C:17]=1[CH3:18]

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 24654Hydrazine hydrate (1:1)HCID 221781542-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrile

생성물 1

HCID 23113351HCID 23113351, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Acetic acid (1.3 ml, 22.36 mmol) was added to a stirred suspension of 2-(2-chloro-4-methoxyphenyl)-3-oxobutanenitrile (2.0 g, 8.94 mmol) and hydrazine hydrate (0.65 ml, 13.41 mmol) in dry toluene (25 ml). The reaction mixture was heated at reflux for 20 h. The solvent was removed in vacuo and the residue was partitioned between 2M HCl and EtOAc. The organic extract was extracted several times with 2M HCl then discarded. The acidic extract was neutralised with NaHCO3 then re-extracted 3× with EtOAc. The combined organic extracts were dried (MgSO4) and the solvent removed to give the title compound as a viscous gum. No further purification was carried out; LCMS: Rt 1.19 mins; [M+H]+ 238.1 1H NMR (400 MHz, d6-DMSO) δ 1.95 (3H, s), 3.80 (3H, s), 4.1 (2H, br m), 6.92 (1H, s), 7.10 (1H, s), 7.20 (1H, d).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 20 h
  3. customThe solvent was removed in vacuo
  4. customthe residue was partitioned between 2M HCl and EtOAc
  5. extractionThe organic extract
  6. extractionwas extracted several times with 2M HCl
  7. extractionThe acidic extract
  8. extractionthen re-extracted 3× with EtOAc
  9. dry with materialThe combined organic extracts were dried (MgSO4)
  10. customthe solvent removed

출처 및 근거

ORD 기록
ord-5759e8e8560147679cbb1c6d4879eabf
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08835444B2

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