Ethyl Acetate → HCID 118874979, 화합물

HRID 60152

반응식

HRID 60152 반응식
[CH3:1][O:2][C:3](=[O:9])[CH2:4][CH2:5]C(O)=O.C1(P([N:24]=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[NH2:27][C:28]1[C:33]([C:34]([OH:36])=[O:35])=[CH:32][C:31]([Cl:37])=[N:30][CH:29]=1.C[C:39](=[O:43])OCC>C1(C)C=CC=CC=1>[Cl:37][C:31]1[CH:32]=[C:33]([C:28]([NH:27][C:39]([NH:24][CH2:5][CH2:4][C:3]([O:2][CH3:1])=[O:9])=[O:43])=[CH:29][N:30]=1)[C:34]([OH:36])=[O:35]

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 77487monoMethyl succinateHCID 199401P,P-Diphenylphosphinic azideHCID 227367915-Amino-2-chloro-isonicotinic acid

생성물 1

HCID 118874979HCID 118874979, 화합물수율 100%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a solution of 4-methoxy-4-oxobutanoic acid (9.7 g, 73.5 mmol) in toluene (368 mL) was added diphenylphosphoryl azide (20.2 g, 73.5 mmol) followed by TEA (12.4 g, 122.7 mmol). The reaction was stirred at RT for 30 min then 5-amino-2-chloroisonicotinic acid (8.47 g, 49 mmol) was added. The reaction was heated at reflux for 6 h, cooled to RT then diluted with EA (300 mL). The mixture was washed with brine (300 mL) and out of the organic layer precipitated a solid which was filtered. The separated aqueous layer was acidified to PH 5 by adding aq. 2N HCl and a precipitate formed. The solid was filtered and combined with the organic layer solid. The combined solids were dried to give 2-chloro-5-(3-(3-methoxy-3-oxopropyl)ureido) isonicotinic acid (26 g, >100% yield) as brown semi-solid. LCMS: MH+ 302 MH+ and TR=2.752 min. Used without further purification.

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 6 h
  3. temperaturecooled to RT
  4. washThe mixture was washed with brine (300 mL) and out of the organic layer
  5. customprecipitated a solid which
  6. filtrationwas filtered
  7. additionby adding aq. 2N HCl
  8. customa precipitate formed
  9. filtrationThe solid was filtered
  10. customThe combined solids were dried

출처 및 근거

ORD 기록
ord-8abc8e802ee14c468c092575131cf8ff
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440973B2

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