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Isobutylamine → Isobutyl-(8-propyl-[1,2,4]triazolo[1,5-c]pyrimidin-7-ylmethyl)-amine

HRID 898708
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HRID 898708 반응식
Br[CH2:2][C:3]1[N:8]=[CH:7][N:6]2[N:9]=[CH:10][N:11]=[C:5]2[C:4]=1[CH2:12][CH2:13][CH3:14].C([O-])([O-])=O.[K+].[K+].[CH2:21]([NH2:25])[CH:22]([CH3:24])[CH3:23]>CC#N>[CH2:21]([NH:25][CH2:2][C:3]1[N:8]=[CH:7][N:6]2[N:9]=[CH:10][N:11]=[C:5]2[C:4]=1[CH2:12][CH2:13][CH3:14])[CH:22]([CH3:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6558IsobutylamineHCID 11430Potassium CarbonateHCID 575033117-Bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine

생성물 1

HCID 58661548Isobutyl-(8-propyl-[1,2,4]triazolo[1,5-c]pyrimidin-7-ylmethyl)-amine

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 7-bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine (16.58 mmol) in CH3CN (30 ml) is added K2CO3 (9.15 g, 66.3 mmol), isobutylamine (6.6 ml, 66.3 mmol) and the mixture is stirred at room temperature overnight. The solvent is removed in vacuo and to the residue is added water (60 ml) and EtOAc (60 ml). The layers are separated and the organic layer is washed with brine (20 ml) and dried (Na2SO4). Evaporation of the solvent provides a light yellow oil, which is used in next step without further purification.

후처리

  1. customThe solvent is removed in vacuo and to the residue
  2. additionis added water (60 ml) and EtOAc (60 ml)
  3. customThe layers are separated
  4. washthe organic layer is washed with brine (20 ml)
  5. dry with materialdried (Na2SO4)
  6. customEvaporation of the solvent
  7. customprovides a light yellow oil, which
  8. customis used in next step without further purification

출처 및 근거

ORD 기록
ord-d18e2a2c015e447f99bc6b735389ae70
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07351826B2

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