Water → Isamoxole

HRID 1112383

反応式

HRID 1112383 の反応式
[CH2:1]([NH:5][C:6]1[O:7][CH:8]=[C:9]([CH3:11])[N:10]=1)[CH2:2][CH2:3][CH3:4].C(N(CC)CC)C.[C:19](Cl)(=[O:23])[CH:20]([CH3:22])[CH3:21].O>C1C=CC=CC=1>[CH2:1]([N:5]([C:6]1[O:7][CH:8]=[C:9]([CH3:11])[N:10]=1)[C:19](=[O:23])[CH:20]([CH3:22])[CH3:21])[CH2:2][CH2:3][CH3:4]

参加物

6

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 62325Isobutyryl chlorideHCID 122952262-Oxazolamine, N-butyl-4-methyl-

生成物 1

HCID 42118Isamoxole収率 80%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

2-(N-butylamino)-4-methyloxazole (106.7 g., 0.69 m.) and triethylamine (110 g., 0.77 m.) were stirred together in dry benzene (1500 c.c.) during the addition of isobutyryl chloride (81.0 g., 0.76 m.). The mixture was stirred at room temperature for 15 hours and then water (1 liter) was added. After stirring for a further hour the organic phase was separated, and the aqueous phase extracted twice in ether. The combined extract was washed successively with 2N hydrochloric acid (2 × 500 c.c.), 10% sodium carbonate solution (2 × 500 c.c.), and saturated brine (2 × 500 c.c.). Evaporation of the dried organic phase gave an oil, which was distilled to give 2-(N-butyl isobutyramido)-4-methyloxazole, (118 g., 80%), b.p. 75°-76° C/0.15 mm., which existed as an oil at room temperature but crystallised on cooling to 0° C.

後処理

  1. stirringAfter stirring for a further hour the organic phase
  2. customwas separated
  3. extractionthe aqueous phase extracted twice in ether
  4. extractionThe combined extract
  5. washwas washed successively with 2N hydrochloric acid (2 × 500 c.c.), 10% sodium carbonate solution (2 × 500 c.c.), and saturated brine (2 × 500 c.c.)
  6. customEvaporation of the dried organic phase
  7. customgave an oil, which
  8. distillationwas distilled

出典と根拠

ORDレコード
ord-70eda08a00a04820bb814dca19d369c3
出典データセット
uspto-grants-1978_10
特許番号
US04122183

関連ノート

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