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Pyridine → 2-(4-Tert-butylphenyl)-6-nitro-3,1-benzoxazin-4-one

HRID 842383
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HRID 842383 반응식
[N+:1]([C:4]1[CH:12]=[C:8]([C:9]([OH:11])=[O:10])[C:7]([NH2:13])=[CH:6][CH:5]=1)([O-:3])=[O:2].N1C=CC=CC=1.[C:20]([C:24]1[CH:32]=[CH:31][C:27]([C:28](Cl)=O)=[CH:26][CH:25]=1)([CH3:23])([CH3:22])[CH3:21].O1C2C=CC=CC=2CC(=O)N1.C(Cl)(=O)C(Cl)=O>CN(C=O)C.C(Cl)Cl>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[N:13]=[C:28]([C:27]3[CH:31]=[CH:32][C:24]([C:20]([CH3:23])([CH3:22])[CH3:21])=[CH:25][CH:26]=3)[O:10][C:9](=[O:11])[C:8]=2[CH:12]=1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 1049PyridineHCID 120322-Amino-5-nitrobenzoic acidHCID 65578Oxalyl chlorideHCID 743724-tert-Butylbenzoyl chlorideHCID 199374482H-1,2-Benzoxazin-3(4H)-one

생성물 1

HCID 3855992-(4-Tert-butylphenyl)-6-nitro-3,1-benzoxazin-4-one수율 93.6%

시약·촉매·용매

2
HCID 6228Dimethylformamide용매2회HCID 6344Dichloromethane용매

실험 절차

To a mixture of 5-nitroanthranilic acid (24.59 g, 135 mmol) and pyridine (14.19 mL, 175.5 mmol, 1.3 eq) in DMF (140 mL) at 0° C., under N2, was added 4-t-butylbenzoyl chloride (31.64 mL, 162 mmol, 1.2 eq) over 15 min. After warming to room temperature, the reaction mixture was heated to 80° C. for 4 h. The reaction mixture was cooled and poured into 700 mL ice-water and stirred to break up the solid material. Filtration, with water followed with 1:2 Et2O:hexane washes, and vacuum drying (150° C./13 Pa/2 h) afforded a light brown solid as a mixture of acid and benzoxazinone (37.1 g, 80%). The solid was suspended in DMF (0.4 mL, 5.4 mmol, 0.05 eq) and methylene chloride (200 mL), under N2, and oxalyl chloride (10.4 mL, 119.2 mmol, 1.1 eq) was added dropwise. Vigorous gas evolution was observed. The solid went into solution over 2 h. The mixture was concentrated to a volume of about 125 mL (cold) in vacuo and filtered to give a light tan solid (about 10 g). A second crop was about 85% pure (about 10 g). The mother liquor was evaporated to dryness and vacuum dried (80° C./13 Pa/3 h) to afford a light brown solid product, 95% pure (about 12 g).

후처리

  1. temperaturethe reaction mixture was heated to 80° C. for 4 h
  2. temperatureThe reaction mixture was cooled
  3. filtrationFiltration
  4. dry with materialhexane washes, and vacuum drying (150° C./13 Pa/2 h)
  5. customafforded a light brown solid
  6. concentrationThe mixture was concentrated to a volume of about 125 mL (cold) in vacuo
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-d1111264cab44a6a9d9d969e8aa93686
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06372759B1

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