Hydrochloric Acid → HCID 54455982, compound

HRID 1416751Notes

Reaction equation

HRID 1416751 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]([OH:29])[CH2:9][NH:10][CH:11]([CH3:28])[CH2:12][C:13]2[CH:27]=[CH:26][C:16]3[O:17][C:18]([C:23]([OH:25])=[O:24])([C:20]([OH:22])=[O:21])[O:19][C:15]=3[CH:14]=2)[CH:5]=[CH:6][CH:7]=1.[CH3:30][CH:31]([CH3:36])[CH2:32][CH2:33][CH2:34]O.Cl.[K+].[Br-]>C(Cl)(Cl)Cl>[CH3:30][CH:31]([CH3:36])[CH2:32][CH2:33][CH2:34][O:24][C:23]([C:18]1([C:20]([O:22][CH2:7][CH2:2][CH2:3][CH:4]([CH3:8])[CH3:5])=[O:21])[O:17][C:16]2[CH:26]=[CH:27][C:13]([CH2:12][CH:11]([NH:10][CH2:9][CH:8]([C:4]3[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=3)[OH:29])[CH3:28])=[CH:14][C:15]=2[O:19]1)=[O:25]

Participants

6

Procedure

The title compound was prepared from 5-{2-[2-(3-chloro-phenyl)-2-hydroxy-ethylamino]-propyl}-benzo[1,3]dioxole-2,2-dicarboxylic acid and 4-methylpentanol according to the procedure of Example 30 as a colorless gum (HCl salt); 1H NMR (CDCl3) δ 0.87 (d, J=6.5 Hz, 12H), 1.33 (bs, 3H), 1.10-2.0 (m, 10H), 2.80 (bs, 1H), 3.18 (bs, 2H), 3.48 (bs, 2H), 4.28(m, 4H), 5.60 (bs, 2H), 6.80 (m, 3H), 7.25 (m, 2H), 7.43 (s, 1H), 8.70 (bs, 1H), 10.10 (bs, 1H); IR (KBr): 1765 cm-1 (C=O); MS (CI) m/z 590 (MH+); [α]D25 -24° (c, 1.0, CHCl3). Anal. Calcd. for C32H44ClNO7HCl: C, 61.34; H, 7.08; N, 2.24; Cl, 11.32. Found: C, 60.50; H, 7.36; N, 2.13; Cl, 11.66.

Sources & evidence

ORD record
ord-977835861e71459993ac1e461e81f690
Source dataset
uspto-grants-1999_06
Patent number
US05914339

Reaction notes

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