반응 #2146724

ord-f82066a6270c4284bf99cbe6bd4b4631

반응 방정식

Cc1cc(C)nc(N(Cc2ccc3cc(CN(C(=O)OC(C)(C)C)c4cc(C)cc(C)n4)ccc3c2)C(=O)OC(C)(C)C)c1
6a
Cc1cc(C)nc(N(Cc2ccc3cc(CN(C(=O)OC(C)(C)C)c4cc(C)cc(C)n4)ccc3c2)C(=O)OC(C)(C)C)c1
Di-tert-butyl naphthalene-2,6-diylbis(methylene)bis(4,6-dimethylpyridin-2-ylcarbamate)
O=C(O)C(F)(F)F
trifluoroacetic acid
Cc1cc(C)nc(NCc2ccc3cc(CNc4cc(C)cc(C)n4)ccc3c2)c1
3a
수율 90.0%
Cc1cc(C)nc(NCc2ccc3cc(CNc4cc(C)cc(C)n4)ccc3c2)c1
N,N′-(Naphthalene-2,6-diylbis(methylene))bis(4,6-dimethylpyridin-2-amine)
수율 90.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축then was concentrated
  2. 2
    기타The crude product was purified by flash column chromatography (2-5% MeOH in CH2Cl2)

실험 절차

To a solution of 6a (590 mg, 1.0 mmol) in CH2Cl2 (8 mL) was added trifluoroacetic acid (TFA, 8 mL) The reaction mixture was allowed to stir at room temperature for 8 h then was concentrated. The crude product was purified by flash column chromatography (2-5% MeOH in CH2Cl2) to yield 3a (355 mg, 90%) as a white solid: 1H NMR (500 MHz, CD3OD/CDCl3) δ 2.28 (s, 6H), 2.48 (s, 6H), 4.60 (s, 4H), 6.46 (s, 4H), 7.45-7.47 (d, J=8.5, 2H), 7.78 (s, 2H), 7.84-7.86 (d, J=8.5, 2H); 13C NMR (125 MHz, CD3OD/CDCl3) δ 18.6, 22.0, 45.9, 106.8, 114.5, 125.6, 129.0, 133.1, 134.3, 147.6, 153.8, 158.0; ESI (M+H+) calcd for C26H29N4 397.23922, found 397.23999.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08278084B2uspto-grants-2012_10