Sulfamic acid[[2,6-bis(1-methylethyl)phenyl]-acetyl]-2,6-bis(1-methylethyl)phenyl ester → HCID 19046528, compound

HRID 2396296Notes

Reaction equation

HRID 2396296 reaction equation
CC(C1C=CC=C(C(C)C)C=1[CH2:13][C:14]([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:15])C.C(C1C=CC=C(C(C)C)C=1CC(O)=O)(C)C.[CH3:49][CH:50]([C:52]1[CH:62]=[C:61]([CH:63]([CH3:65])[CH3:64])[CH:60]=[C:59]([CH:66]([CH3:68])[CH3:67])[C:53]=1[O:54]CC(O)=O)[CH3:51]>>[CH3:68][CH:66]([C:59]1[CH:60]=[C:61]([CH:63]([CH3:65])[CH3:64])[CH:62]=[C:52]([CH:50]([CH3:51])[CH3:49])[C:53]=1[O:54][CH2:13][C:14]([C:16]1[C:17]([CH:30]([CH3:31])[CH3:32])=[C:18]([O:25][S:26](=[O:28])(=[O:29])[NH2:27])[C:19]([CH:22]([CH3:23])[CH3:24])=[CH:20][CH:21]=1)=[O:15])[CH3:67]

Participants

4

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 [2,4,6-tris(1-methylethyl)phenoxy]acetic acid, mp 126°-128° C.

Sources & evidence

ORD record
ord-094bea6520744f3c8468572a64732941
Source dataset
uspto-grants-1996_02
Patent number
US05491172

Reaction notes

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