反应 #2446114

ord-50f7af91c1e24a149147b554c3192051

反应方程式

NCCCCCCCCNCCCCCCCCN
1,17-diamino-9-azaheptadecane
CSC(=NC(=O)OC(C)(C)C)NC(=O)OC(C)(C)C
N,N′-bis(tert-butoxycarbonyl)-S-methylisothiourea
CC(C)(C)OC(=O)N=C(NCCCCCCCCNCCCCCCCCN)NC(=O)OC(C)(C)C
12
CC(C)(C)OC(=O)N=C(NCCCCCCCCNCCCCCCCCN)NC(=O)OC(C)(C)C
1-amino-17-[N2,N3-bis(tert-butoxycarbonyl)guanidino]-9-azaheptadecane

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩the reaction mixture was concentrated under reduced pressure
  2. 2
    其他the residue was purified by flash chromatography (6% methanol, 4% triethylamine, 90% ethyl acetate)

实验过程

To a stirred solution of 1,17-diamino-9-azaheptadecane 3 (4.9 g, 15.06 mmol) in THF/CH3OH 5/3 (80 mL) at 50° C., a solution of N,N′-bis(tert-butoxycarbonyl)-S-methylisothiourea (1.456 g, 5.02 mmol) in THF (25 mL) was added dropwise over 1 h. After 16 h, the reaction mixture was concentrated under reduced pressure and the residue was purified by flash chromatography (6% methanol, 4% triethylamine, 90% ethyl acetate), affording 12 as a pale yellow oil, 3.51 g (70%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08685953B2uspto-grants-2014_04