反応 #531856

ord-04fef6ade7b04310ac15b1c8322e858b

反応方程式

Cl
HCl
NCCCC(=O)O
4-aminobutyric acid
CN(C)C=O
DMF
O=C=NC12CC3CC(CC(C3)C1)C2
1-adamantyl isocyanate
O=C(O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
4-(3-adamantan-1-yl-ureido)butyric acid
収率 100.0%
COC(=O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
title compound
COC(=O)CCCNC(=O)NC12CC3CC(CC(C3)C1)C2
4-(3-Adamantan-1-yl-ureido) butyric Acid Methyl Ester

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe mixture was stirred for 30 min
  2. 2
    ろ過The solid crystalline product was filtered
  3. 3
    洗浄washed with water (20 mL) and ethyl acetate (20 mL)
  4. 4
    その他The resulting solid was dried in a vacuum oven

実験手順

The title compound was prepared by a procedure described in J. Med. Chem. 2004, 47, 2110. To a suspension of 4-aminobutyric acid (2.79 g, 27.1 mmol) in DMF (40 mL) was added 1-adamantyl isocyanate (1.20 g, 6.77 mmol) at room temperature. The reaction mixture was stirred for 24 h. Then 1 N HCl aqueous solution (40 mL) was added into the reaction, and the mixture was stirred for 30 min. The solid crystalline product was filtered and washed with water (20 mL) and ethyl acetate (20 mL). The resulting solid was dried in a vacuum oven to give 1.90 g (100%) of 4-(3-adamantan-1-yl-ureido)butyric acid 822 as a white solid: 1H NMR (CD3OD): 1.66-1.75 (8H, m), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.30 (2H, t, J=6.9 Hz), 3.08 (2H, q, J=6.9 Hz), 3.32 (2H, s); LC-MS (ESI) m/z calcd for C15H24N2O3 [M+H]+ 281.18. found [M+H]+ 281.25; mp 165 C. Anal. (C15H24N2O3) C, H, N.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08476043B2uspto-grants-2013_07