HCID 19996065, compound → HCID 19996126, compound

HRID 359753Notes

Reaction equation

HRID 359753 reaction equation
[NH2:1][C:2]1[C:7]([Cl:8])=[CH:6][C:5]([CH:9]([OH:34])[CH2:10][NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][CH2:21][C:22]2[O:26][C:25]([C:27]([N:29]([CH2:32][CH3:33])[CH2:30][CH3:31])=O)=[CH:24][CH:23]=2)=[CH:4][C:3]=1[Cl:35].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1C=CC=CC=1.CCOCC>[NH2:1][C:2]1[C:7]([Cl:8])=[CH:6][C:5]([CH:9]([CH2:10][NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][CH2:21][C:22]2[O:26][C:25]([CH2:27][N:29]([CH2:30][CH3:31])[CH2:32][CH3:33])=[CH:24][CH:23]=2)[OH:34])=[CH:4][C:3]=1[Cl:35]

Participants

5

Procedure

A solution of 5-[3-[[6-[[2-(4-amino-3,5-dichlorophenyl)-2-hydroxyethyl]amino]hexyl]oxy]propyl]-N,N-diethyl-2-furancarboxamide (0.83 g) in benzene (6 ml) was added dropwise over 10 min to a stirred suspension of lithium aluminium hydride (175 mg) in dry ether (15 ml) under nitrogen. The mixture was stirred under nitrogen at 22° for 24 h, then quenched sequentially with water (1 ml), 2N sodium hydroxide solution (1 ml) and water (2 ml). The mixture was filtered through hyflo and the solids washed with toluene-ether (1:1, 10 ml). The combined filtrate and washings were dried and evaporated in vacuo to an oil. Purification by FCC eluting with System C (93:5:2) afforded the title compound as a pale yellow oil (0.59 g), t.l.c. (System A 39:10:1) Rf 0.5.

Workup

  1. customquenched sequentially with water (1 ml), 2N sodium hydroxide solution (1 ml) and water (2 ml)
  2. filtrationThe mixture was filtered through hyflo
  3. washthe solids washed with toluene-ether (1:1, 10 ml)
  4. customThe combined filtrate and washings were dried
  5. customevaporated in vacuo to an oil
  6. customPurification by FCC
  7. washeluting with System C (93:5:2)

Sources & evidence

ORD record
ord-45ca254ab04d404996f1a12437a3b2a8
Source dataset
uspto-grants-1991_03
Patent number
US05002966

Reaction notes

Loading…