반응 #487709

ord-78a50519fe824b13a5f863a7acb6edb0

반응 방정식

Nc1cc(C(=O)O)ccc1F
3-amino-4-fluorobenzoic acid
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
CCN=C=NCCCN(C)C
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
C1C[C@@H]2CNCCN2C1
(R)-octahydropyrrolo[1,2-a]pyrazine
Nc1cc(C(=O)N2CCN3CCC[C@@H]3C2)ccc1F
(R)-(3-amino-4-fluorophenyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)methanone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축Then the mixture was concentrated
  2. 2
    기타The residue was purified by chromatography on silica gel (dichloromethane

실험 절차

To 3-amino-4-fluorobenzoic acid (0.621 g, 4 mmol) and 1-hydroxybenzotriazole hydrate (0.613 g, 4 mmol) in dichloromethane/N,N-dimethylformamide (10:1, 60 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC, 0.621 g, 4 mmol). After 5 minutes, (R)-octahydropyrrolo[1,2-a]pyrazine (0.505 g, 4 mmol) in dichloromethane (1 mL) was added. The mixture was stirred at room temperature overnight. Then the mixture was concentrated. The residue was purified by chromatography on silica gel (dichloromethane, then methanol/dichloromethane=1:10) to give (R)-(3-amino-4-fluorophenyl)(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)methanone: 1H NMR (500 MHz, DMSO-d6) δ ppm 1.25 (m, 1H), 1.60-2.10 (m, 6H), 2.70-3.10 (m, 4H), 3.55-3.70 (m, 1H), 4.40-4.60 (m, 1H), 5.30 (s, 2H), 6.50 (m, 1H), 6.77 (m, 1H), 7.00 (m, 1H); MS (ESI) m/z 264 (M+H)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08741899B2uspto-grants-2014_06