[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:41]=[CH:40][C:20]3[C:21](=[O:39])[CH2:22][C:23]([CH2:32][CH2:33][C:34]([O:36]CC)=[O:35])([CH2:25][CH2:26][C:27]([O:29]CC)=[O:28])[O:24][C:19]=3[C:18]=2[CH2:42][CH2:43][CH3:44])=[CH:4][CH:3]=1.ClC1C=CC(OCCCOC2C=CC3C(=O)CC(CCC(OCC)=O)(CCC(OCC)=O)OC=3C=2CCC)=CC=1>C(OCC)C>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]2[CH:41]=[CH:40][C:20]3[C:21](=[O:39])[CH2:22][C:23]([CH2:32][CH2:33][C:34]([OH:36])=[O:35])([CH2:25][CH2:26][C:27]([OH:29])=[O:28])[O:24][C:19]=3[C:18]=2[CH2:42][CH2:43][CH3:44])=[CH:4][CH:3]=1The title compound was prepared by the method of Example 22 substituting the title product of Example 34 (515 mg) for the title product of Example 21 to give, after trituration with diethylether, 352 mg as a solid, m.p. 170.5°-171° C.
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