Xanthene-9-carboxylic acid → HCID 18988687, compound

HRID 2396286Notes

Reaction equation

HRID 2396286 reaction equation
CC(C1C=CC=C(C(C)C)C=1CC([C:16]1[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:29])(=[O:28])[NH2:27])[C:19]([CH:22]([CH3:24])[CH3:23])=[CH:20][CH:21]=1)=O)C.C(C1C=CC=C(C(C)C)C=1CC(O)=O)(C)C.[CH:49]1[C:62]2[CH:61]([C:63](O)=[O:64])[C:60]3[C:55](=[CH:56][CH:57]=[CH:58][CH:59]=3)[O:54][C:53]=2[CH:52]=[CH:51][CH:50]=1>>[CH:59]1[C:60]2[CH:61]([C:63]([C:16]3[C:17]([CH:30]([CH3:32])[CH3:31])=[C:18]([O:25][S:26](=[O:28])(=[O:29])[NH2:27])[C:19]([CH:22]([CH3:24])[CH3:23])=[CH:20][CH:21]=3)=[O:64])[C:62]3[C:53](=[CH:52][CH:51]=[CH:50][CH:49]=3)[O:54][C:55]=2[CH:56]=[CH:57][CH:58]=1

Participants

4

Reactant 3

HCID 65736Xanthene-9-carboxylic acidHCID 10226443Sulfamic acid[[2,6-bis(1-methylethyl)phenyl]-acetyl]-2,6-bis(1-methylethyl)phenyl esterHCID 152779902-(2,6-Diisopropylphenyl)acetic acid

Product 1

HCID 18988687HCID 18988687, compound

Procedure

This compound was prepared in the same manner as for the title compound of Example 1, except that 2,6-diisopropylphenylacetic acid was replaced with xanthene-9-carboxylic acid, mp 180°-181° C.

Sources & evidence

ORD record
ord-a92026c49b4041058ef380fcbf0d9d6a
Source dataset
uspto-grants-1996_02
Patent number
US05491172

Reaction notes

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