반응 #1857597

ord-2f39b7eda67447c8892b537e6adfb097

반응 방정식

Oc1cccc2[nH]nnc12
hydroxybenzotriazole
NC(CO)(CO)CO
Trisamine
Cc1noc(C)c1Cn1cc(N)cn1.Cl
1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-amine hydrochloride
Oc1cccc2[nH]nnc12
Hydroxybenzotriazole
O=C(O)c1ccc2c(c1)OCO2
benzo[d][1,3]dioxole-5-carboxylic acid
Cc1noc(C)c1Cn1cc(NC(=O)c2ccc3c(c2)OCO3)cn1
desired product
수율 6.0%
Cc1noc(C)c1Cn1cc(NC(=O)c2ccc3c(c2)OCO3)cn1
N-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)benzo[d][1,3]dioxole-5-carboxamide
수율 6.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added into the reaction well
  2. 2
    workup.ADDITIONwas added into the reaction mixture
  3. 3
    workup.WAITto shake overnight at room temperature
  4. 4
    workup.STIRRINGshaken for 1 minute
  5. 5
    기타The solution was evaporated under vacuum

실험 절차

1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-amine hydrochloride (example 1a) (8 mg, 35 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (7 mg, 42 μmol) were each dissolved in 200 uL dimethylformamide. Si-Carbodiimide resin (70 mg, 70 μmol) was loaded into a 1.2 mL 96 well Greiner plate, followed by the addition of amine and acid. Hydroxybenzotriazole (6 mg, 42 μmol) was dissolved in 100 uL dimethylformamide and was added into the reaction well. The reaction was shaken overnight at room temperature. To remove excess carboxylic acid and hydroxybenzotriazole, PS-Trisamine resin (35 mg, 70 μmol) was added into the reaction mixture and was allowed to shake overnight at room temperature. 200 uL of Acetonitrile was added into the reaction well and shaken for 1 minute. The top clear solution was transferred into a new plate. The extraction process was repeated two more times. The solution was evaporated under vacuum and gave the desired product. Yield 6%. MS M+H calculated 341.1. Found 341.2.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09247759B2uspto-grants-2016_02