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Phosphorus pentachloride → 2-(4-Methyl-1-piperazinyl)-5-nitrobenzoxazole

HRID 2270951
ノート
印刷プレビュー

反応式

HRID 2270951 の反応式
P(Cl)(Cl)(Cl)(Cl)Cl.S[C:8]1[O:9][C:10]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:11]=2[N:12]=1.[CH3:20][N:21]1[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]1>C1(C)C=CC=CC=1>[CH3:20][N:21]1[CH2:26][CH2:25][N:24]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:11]=3[N:12]=2)[CH2:23][CH2:22]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24819Phosphorus pentachlorideHCID 531671-MethylpiperazineHCID 178526504HCID 178526504、化合物

生成物 1

HCID 225581882-(4-Methyl-1-piperazinyl)-5-nitrobenzoxazole

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
100 °C

実験手順

Phosphorus pentachloride (1.37 g) was dissolved in anhydrous toluene (18 ml), the resulting solution was mixed with 2-mercapto-5-nitrobenzoxazole (900 mg) which has been obtained in the same manner as described in Reference Example 1, and the mixture was then stirred with heating at 100° C. for 3 hours. With cooling in an ice bath, to this was added dropwise N-methylpiperazine (6.09 ml). After 20 minutes of stirring, the thus obtained mixture was extracted with ethyl acetate, and the organic layer was washed with saturated sodium bicarbonate aqueous solution and saturated brine in that order. After drying with magnesium sulfate, the solvent was evaporated under a reduced pressure, and the resulting residue was purified by a silica gel column chromatography (methylene chloride:methanol=10:1) to obtain 2-(4-methyl-1-piperazinyl)-5-nitrobenzoxazole (56.1 mg) in the form of yellow crystalline powder.

後処理

  1. customhas been obtained in the same manner
  2. temperatureWith cooling in an ice bath
  3. stirringAfter 20 minutes of stirring
  4. extractionthe thus obtained mixture was extracted with ethyl acetate
  5. washthe organic layer was washed with saturated sodium bicarbonate aqueous solution and saturated brine in that order
  6. dry with materialAfter drying with magnesium sulfate
  7. customthe solvent was evaporated under a reduced pressure
  8. customthe resulting residue was purified by a silica gel column chromatography (methylene chloride:methanol=10:1)

出典と根拠

ORDレコード
ord-7a594448f2754caba92d65dd2420c913
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06333328B1

反応ノート

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