Acetic Acid → (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(5-chloro-2-methoxyphenyl)acrylate

HRID 75532

반응식

HRID 75532 반응식
C[O-].[Na+].Cl.[NH2:5][CH2:6][C:7]([NH2:9])=[O:8].C(O)(=O)C.[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([O:29][CH3:30])=[C:19]([C:21](=O)[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH:20]=1>CO>[NH2:9][C:7](=[O:8])[CH2:6][NH:5]/[C:21](/[C:19]1[CH:20]=[C:15]([Cl:14])[CH:16]=[CH:17][C:18]=1[O:29][CH3:30])=[CH:22]\[C:23]([O:25][CH2:26][CH3:27])=[O:24]

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 2723639Glycinamide hydrochlorideHCID 10942334Sodium MethoxideHCID 54012347Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate

생성물 1

HCID 86684671(Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(5-chloro-2-methoxyphenyl)acrylate수율 105.4%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
65 °C

실험 절차

A 5-L reaction vessel was charged with methanol (3.3 L), sodium methoxide (102.4 g, 1.8 moles), and glycinamide hydrochloride (202 g, 1.8 moles). The mixture was heated at 65° C. for 1 hour before cooling to 50° C. and adding acetic acid (514.25 mmoles, 30.88 g, 29.47 mL) and ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate (300 g, 1.03 mole). After heating to reflux for 16 hours, the reaction mixture was stirred as it was cooled to 10° C. After 30 min the resulting solid was collected by vacuum filtration, pulling dry to form a cake that was dried in a vacuum oven (20 mm Hg, 65° C.) for 14 hours to afford the title compound (339.4 g).

후처리

  1. temperaturebefore cooling to 50° C.
  2. temperatureAfter heating
  3. temperatureto reflux for 16 hours
  4. temperaturewas cooled to 10° C
  5. filtrationAfter 30 min the resulting solid was collected by vacuum filtration
  6. custompulling dry
  7. customto form a cake that
  8. customwas dried in a vacuum oven (20 mm Hg, 65° C.) for 14 hours

출처 및 근거

ORD 기록
ord-3ab8f49f91f44ae7a68cebd6e8502594
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08835449B2

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