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Neopentylamine → HCID 19428493, 화합물

HRID 1078292
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HRID 1078292 반응식
[NH2:1][CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4].[Cl:7][C:8]1[CH:13]=[C:12](Cl)[N:11]=[C:10]([NH:15][CH2:16][C:17]([CH3:20])([CH3:19])[CH3:18])[N:9]=1>C(O)(C)C>[Cl:7][C:8]1[CH:13]=[C:12]([NH:1][CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4])[N:11]=[C:10]([NH:15][CH2:16][C:17]([CH3:20])([CH3:19])[CH3:18])[N:9]=1
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참가 물질

4

반응물 2

HCID 79882NeopentylamineHCID 19428516HCID 19428516, 화합물

생성물 1

HCID 19428493HCID 19428493, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

After adding 5 ml of 1-amino-2,2-dimethylpropane to a solution of 5.0 g of 4,6-dichloro-2-(2,2-dimethylpropylamino)pyrimidine in 25 ml of isopropanol the reaction mixture is boiled under reflux for 20 hours, then evaporated. The residue is distributed between 80 ml of chloroform and 15 ml of 10% sodium hydroxide solution. After separation the organic phase is washed 4 times with 20 ml of water each, then dried and evaporated. After recrystallization from hexane the title compound is obtained in a yield of 2.994 g (49.4%), m.p.:95°-98° C.

후처리

  1. temperatureunder reflux for 20 hours
  2. customevaporated
  3. customAfter separation the organic phase
  4. washis washed 4 times with 20 ml of water each,
  5. customthen dried
  6. customevaporated
  7. customAfter recrystallization from hexane the title compound
  8. customis obtained in a yield of 2.994 g (49.4%), m.p.:95°-98° C.

출처 및 근거

ORD 기록
ord-8d36710408eb48b587c3d9f84f146860
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05547949

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