HCID 10279786, compound → HCID 19046538, compound

HRID 2396262Notes

Reaction equation

HRID 2396262 reaction equation
[CH3:1][CH:2]([C:4]1[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[CH:7]=[C:6]([CH:13]([CH3:15])[CH3:14])[C:5]=1[CH2:16][C:17]([C:19]1[C:20]([CH:33]([CH3:35])[CH3:34])=[C:21]([O:28][S:29](=[O:32])(=[O:31])[NH2:30])[C:22]([CH:25]([CH3:27])[CH3:26])=[CH:23][CH:24]=1)=[O:18])[CH3:3].[CH:36](C1C=CC=C(C(C)C)C=1OS(N=C=O)(=O)=O)([CH3:38])[CH3:37].C(C1C=C(C(C)C)C=C(C(C)C)C=1OS(N=C=O)(=O)=O)(C)C>>[CH3:3][CH:2]([C:4]1[CH:9]=[C:8]([CH:10]([CH3:11])[CH3:12])[CH:7]=[C:6]([CH:13]([CH3:14])[CH3:15])[C:5]=1[CH2:16][C:17]([C:19]1[C:20]([CH:33]([CH3:35])[CH3:34])=[C:21]([O:28][S:29](=[O:31])(=[O:32])[NH2:30])[C:22]([CH:25]([CH3:27])[CH3:26])=[CH:23][C:24]=1[CH:36]([CH3:38])[CH3:37])=[O:18])[CH3:1]

Participants

4

Reactant 3

HCID 10279786HCID 10279786, compoundHCID 10636716AG-G-92061HCID 19046536HCID 19046536, compound

Product 1

HCID 19046538HCID 19046538, compound

Procedure

This compound was prepared in the same manner as the title compound of Example 5, except that 2,6-diisopropylphenoxy sulfonyl isocyanate was replaced with 2,4,6-triisopropylphenoxy sulfonyl isocyanate, mp 178°-180° C.

Sources & evidence

ORD record
ord-20cc6eaea9c54f9398d41d37afc8f87a
Source dataset
uspto-grants-1996_02
Patent number
US05491172

Reaction notes

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