Sodium Iodide → HCID 19389035, compound

HRID 1757798Notes

Reaction equation

HRID 1757798 reaction equation
[CH2:1]([O:19][C:20]1[CH:21]=[C:22]([NH2:26])[CH:23]=[CH:24][CH:25]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].Br[CH2:28][C:29]([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30].CN(C)[C:41]1[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][C:49]=2N(C)C)C=CC=1.[I-].[Na+]>C(#N)C.CN(C=O)C>[C:33]1([CH2:32][O:31][C:29](=[O:30])[CH2:28][N:26]([C:22]2[CH:23]=[CH:24][CH:25]=[C:20]([O:19][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH:21]=2)[CH2:28][C:29](=[O:30])[O:31][CH2:41][C:50]2[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=2)[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1

Participants

7

Procedure

A mixture of 5.5 g (0.015 mol) of 3-(octadecyloxy)benzenamine, 7.3 ml (0.046 mol) of benzyl bromoacetate, 8.2 g (0.038 mol) of 1,8-bis(dimethylamino)naphthalene, 0.64 g (4.26 mmol) of sodium iodide in 100 ml of anhydrous acetonitrile and 25 ml of anhydrous DMF was stirred atreflux under an argon atmosphere for 48 hours. The solvents were removed atreduced pressure and the residue was dissolved in ethyl acetate and washed with 0.05N HCl, with saturated NaHCO3 solution dried and concentratedat reduced pressure. Purification by HPLC using 15% ethyl acetate-hexane gave, after recrystallization of the combined pure fractions from ether-hexane, 6.56 g (69% yield, mp 55°-57°) of N-[3-(octadecyloxy)phenyl]-N-[2-oxo-2-(phenylmethoxy)ethyl]glycine phenylmethyl ester.

Workup

  1. customThe solvents were removed
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washwashed with 0.05N HCl, with saturated NaHCO3 solution
  4. customdried
  5. customPurification by HPLC
  6. customgave

Sources & evidence

ORD record
ord-22d5491e9f614d9ea2f866f852730dfe
Source dataset
uspto-grants-1995_08
Patent number
US05446189

Reaction notes

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