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Ammonia → HCID 11381609, 화합물

HRID 558337
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HRID 558337 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:23])[C:10]2[CH:11]=[C:12]([CH:17]=[CH:18][C:19]=2[N+:20]([O-:22])=[O:21])[C:13](OC)=[O:14])=[CH:4][CH:3]=1.[NH3:24]>CO>[N+:20]([C:19]1[CH:18]=[CH:17][C:12]([C:13]([NH2:24])=[O:14])=[CH:11][C:10]=1[C:9]([NH:8][C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=1)=[O:23])([O-:22])=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 23141392HCID 23141392, 화합물

생성물 1

HCID 11381609HCID 11381609, 화합물수율 23%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C

실험 절차

Methyl N-(4-chlorophenyl)-4-nitroisophthalamate (220 mg) obtained in step A was dissolved in 10 mL of a methanol solution of 7 mols of ammonia. After the reactor was sealed, the solution was heated for 36 hours at 80° C. with stirring. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography. The resulting solid was dried under reduced pressure to obtain 48 mg (23%) of 4-nitro-3-N-(4-chlorophenyl)-isophthalamide.

후처리

  1. customAfter the reactor was sealed
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customthe residue was purified by silica gel column chromatography
  4. customThe resulting solid was dried under reduced pressure

출처 및 근거

ORD 기록
ord-fec013549d304448a478d1599a985313
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063046B2

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