反応 #539435

ord-a362e89873744c2ba75f0d3ac6d270da

反応方程式

CC1(C)CC(N)c2ccccc2O1
Intermediate 2
CC1(C)CC(N)c2ccccc2O1
2,2-Dimethylchroman-4-amine
COc1ccc(CC(=O)O)cc1OC
3,4-dimethoxyphenylacetic acid
CCN=C=NCCCN(C)C.Cl
EDCI.HCl
On1nnc2ccccc21
HOBt
CCN(CC)CC
triethylamine
COc1ccc(CC(=O)NC2CC3(CCC3)Oc3ccc(Cl)cc32)cc1OC
title compound
COc1ccc(CC(=O)NC2CC3(CCC3)Oc3ccc(Cl)cc32)cc1OC
N-(6-Chloro-3,4-dihydrospiro[chromene-2,1′-cyclobutan]-4-yl)-2-(3,4-dimethoxyphenyl)acetamide

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

The title compound was prepared from Intermediate 2 (200 mg, 0.763 mmol) and 3,4-dimethoxyphenylacetic acid (224 mg, 1.145 mmol) in presence of EDCI.HCl (219 mg, 1.145 mmol), HOBt (175 mg, 1.145 mmol) and triethylamine (425 μl, 3.053 mmol) in dichloromethane (10 ml) as described in Example 1 to give 217 mg of the product as a white solid; IR (KBr) 3232, 2938, 1634, 1478, 1241, 813 cm−1; 1H NMR (300 MHz, CDCl3) δ 1.62-1.70 (m, 2H), 1.87-1.90 (m, 2H), 1.99-2.15 (m, 2H), 2.18-2.37 (m, 2H), 3.60 (q, J=16.2 Hz, 2H), 3.85 (s, 6H), 5.23 (q, J=9.6 Hz, 1H), 5.48 (d, J=9.0 Hz, 1H), 6.68 (d, J=9.0 Hz, 1H), 6.77-6.84 (m, 3H), 6.96 (s, 1H), 7.04 (d, J=8.4 Hz, 1H); ESI-MS (m/z) 401.27 (100%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08487121B2uspto-grants-2013_07