反応 #1596962

ord-2c7742aaa236405882ca39dc889355b0

反応方程式

CC(C)(C)OC(=O)NCCCCCCCCN
tert-butyl 8-aminooctylcarbamate
O=Cc1ccccn1
2-pyridinecarboxaldehyde
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
NaBH(OAc)3
CC(C)(C)OC(=O)C=O
tert-butyl glyoxalate
CC(C)(C)OC(=O)CN(CCCCCCCCNC(=O)OC(C)(C)C)Cc1ccccn1
tert-butyl 2-((8-(tert-butoxycarbonylamino)octyl)(pyridin-2-ylmethyl)amino)acetate
収率 58.0%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他quenched with water
  2. 2
    抽出The reaction mixture was then extracted with DCM
  3. 3
    その他the organic layers was dried
  4. 4
    濃縮concentrated under reduced pressure
  5. 5
    その他The residue was purified by flash chromatography over silica gel

実験手順

A solution of tert-butyl 8-aminooctylcarbamate (1.61 g, 6.588 mmol), 2-pyridinecarboxaldehyde (0.63 mL, 6.588 mmol) and AcOH (0.10 mL) in DCE (30 mL) was heated at 75° C. for 30 min under nitrogen. The reaction mixture was cooled to 0° C., and treated sequentially with NaBH(OAc)3 (3.708 g, 17.5 mmol) and tert-butyl glyoxalate (1.53 g)1. The reaction mixture was stirred at room temperature overnight and quenched with water. The reaction mixture was then extracted with DCM and the organic layers was dried and concentrated under reduced pressure. The residue was purified by flash chromatography over silica gel to afford tert-butyl 2-((8-(tert-butoxycarbonylamino)octyl)(pyridin-2-ylmethyl)amino)acetate (1.71 g, 58%) as a yellow oil. 1H NMR (400 MHz, CD3Cl3) δ 8.52 (d, J=4.8 Hz, 1H), 7.65 (td, J=7.8, 1.6 Hz, 1H), 7.56 (d, J=7.6, 1H), 7.18-7.12 (m, 1H), 4.50 (s, 1H), 3.90 (s, 2H), 3.28 (s, 2H), 3.07 (q, J=6.3 Hz, 2H), 2.61 (t, J=7.6 Hz, 2H), 1.50-1.24 (m, 30H); ESMS m/z: 450.4 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08211402B2uspto-grants-2012_07