반응 #68650

ord-0656311fd0534041882802a5c7ec95a5

반응 방정식

c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1
BINAP
CC(C)(C)[O-].[Na+]
sodium tert-butoxide
Clc1ccnc2cc(Br)cnc12
3-bromo-8-chloro-1,5-naphthyridine
N=C(c1ccccc1)c1ccccc1
diphenylmethanimine
Clc1ccnc2cc(N=C(c3ccccc3)c3ccccc3)cnc12
8-chloro-N-(diphenylmethylene)-1,5-naphthyridin-3-amine
수율 50.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A 25 ml round bottom flask set up under nitrogen
  2. 2
    workup.ADDITIONwere added
  3. 3
    기타This was placed in a preheated oil bath at 80° C.
  4. 4
    기타Reaction
  5. 5
    기타Filtrate collected
  6. 6
    농축was concentrated
  7. 7
    기타to afford brown oil
  8. 8
    기타This was purified by ISCO silica gel chromatography (40 g, 1% MeOH/DCM over 50 mins)

실험 절차

A 25 ml round bottom flask set up under nitrogen was charged with Pd2(dba)3 (301 mg, 0.33 mmol), BINAP (614 mg, 0.99 mmol) and sodium tert-butoxide (237 mg, 2.46 mmol). System was purged with Argon and 3-bromo-8-chloro-1,5-naphthyridine (400 mg, 1.64 mmol), diphenylmethanimine (0.28 mL, 1.64 mmol), and toluene (1M, 1.64 mL) were added. This was placed in a preheated oil bath at 80° C. and stirred at this temperature for 16 hours. Reaction cooled to room temperature, diluted with dichloromethane, and passed over a celite cake. Filtrate collected was concentrated to afford brown oil. This was purified by ISCO silica gel chromatography (40 g, 1% MeOH/DCM over 50 mins) to afford clean 8-chloro-N-(diphenylmethylene)-1,5-naphthyridin-3-amine (280 mg, 50% yield). MS[M+H]=344.0. Calc'd for C21H14ClN3=343.8.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08524900B2uspto-grants-2013_09