Hydrochloric Acid → HCID 19822245, compound

HRID 1030392Notes

Reaction equation

HRID 1030392 reaction equation
C([O:5][C:6]([CH2:8][O:9][C:10]1[C:11]([CH3:55])=[C:12]2[C:17](=[C:18]([CH3:21])[C:19]=1[CH3:20])[O:16][C:15]([CH2:23][O:24][C:25]1[CH:54]=[CH:53][C:28]([CH2:29][C:30]3([CH2:45][C:46]([O:48]C(C)(C)C)=[O:47])[S:34][C:33](=[O:35])[N:32]([CH2:36][C:37]([O:39]C(C)(C)C)=[O:38])[C:31]3=[O:44])=[CH:27][CH:26]=1)([CH3:22])[CH2:14][CH2:13]2)=[O:7])(C)(C)C.Cl>O1CCOCC1>[C:6]([CH2:8][O:9][C:10]1[C:11]([CH3:55])=[C:12]2[C:17](=[C:18]([CH3:21])[C:19]=1[CH3:20])[O:16][C:15]([CH2:23][O:24][C:25]1[CH:54]=[CH:53][C:28]([CH2:29][C:30]3([CH2:45][C:46]([OH:48])=[O:47])[S:34][C:33](=[O:35])[N:32]([CH2:36][C:37]([OH:39])=[O:38])[C:31]3=[O:44])=[CH:27][CH:26]=1)([CH3:22])[CH2:14][CH2:13]2)([OH:7])=[O:5]

Participants

4

Procedure

A mixture of 0.41 g of di-t-butyl α,α'-{5-[4-(6-t-butoxycarbonylmethoxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]-2,4-dioxothiazolidine-3,5-diyl}diacetate (prepared as described in Example 47) and 4 ml of a 4N dioxane solution of hydrogen chloride was allowed to stand at room temperature overnight. At the end of this time, the reaction mixture was treated in the same manner described in Example 61, to give the title compound as a pale yellow powder, softening at 105°-110° C.

Workup

  1. additionAt the end of this time, the reaction mixture was treated in the same manner

Sources & evidence

ORD record
ord-bf6308bf3e0b468899d766c0c1a05625
Source dataset
uspto-grants-1992_04
Patent number
US05104888

Reaction notes

Loading…