반응 #66303

ord-febcc2bbf55a49ebae7f0dc6f20e7b7e

반응 방정식

CCCNCCC
dipropylamine
[CH3][Al]([CH3])[CH3]
AlMe3
O=C([O-])[C@H](O)[C@@H](O)C(=O)[O-].[K+].[Na+]
Rochelle's salt
CCOC(=O)C1=Cc2ccc(Br)cc2N=C(N)C1
(1E,4E)-ethyl 2-amino-8-bromo-3H-benzo[b]azepine-4-carboxylate
CCCN(CCC)C(=O)C1=Cc2ccc(Br)cc2N=C(N)C1
(1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamide
수율 34.1%

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A 50 ml round bottom flask equipped with a stir bar and nitrogen inlet
  2. 2
    workup.ADDITIONOnce the addition
  3. 3
    온도to warm to room temperature (˜20-30 minutes)
  4. 4
    기타resulting in a dark solution
  5. 5
    온도This mixture was warmed to 100° C. for about 16 hours
  6. 6
    온도to cool to room temperature
  7. 7
    추출extracted with EtOAc (2×)
  8. 8
    건조extracts dried over sodium sulfate
  9. 9
    농축concentrated under reduced pressure

실험 절차

A 50 ml round bottom flask equipped with a stir bar and nitrogen inlet was charged with 15 mls of dry toluene and dipropylamine (0.44 ml, 3.24 mmol). This was chilled to 0° C. and AlMe3 (4.04 mls, 8.09 mmol, 2M in toluene) was then added. Once the addition was complete, the mixture was allowed to warm to room temperature (˜20-30 minutes). (1E,4E)-ethyl 2-amino-8-bromo-3H-benzo[b]azepine-4-carboxylate (0.5 g, 1.62 mmol) was then added portionwise resulting in a dark solution. This mixture was warmed to 100° C. for about 16 hours, and then allowed to cool to room temperature. This mixture was then poured into 50 mls of a 30% aq. solution of Rochelle's salt and vigorously stirred for 20 minutes, then extracted with EtOAc (2×), extracts dried over sodium sulfate and concentrated under reduced pressure. Flash 40 Biotage (40M cartridge, 5% MeOH/DCM) afforded 201 mgs (32%) of (1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamide. m/z (APCI-pos) M+1=364.2, 366.2.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08524702B2uspto-grants-2013_09