Trichloroisocyanuric Acid → HCID 58951824, compound

HRID 254574Notes

Reaction equation

HRID 254574 reaction equation
[CH:1]([C:4]1[CH:15]=[CH:14][CH:13]=[C:12]([CH:16]([CH3:18])[CH3:17])[C:5]=1[CH2:6][C:7]1[NH:8][CH2:9][CH2:10][N:11]=1)([CH3:3])[CH3:2].C1(N(Cl)C(=O)N(Cl)C(=O)N1Cl)=O.C1CCN2C(=NCCC2)CC1>>[CH:1]([C:4]1[CH:15]=[CH:14][CH:13]=[C:12]([CH:16]([CH3:18])[CH3:17])[C:5]=1[CH2:6][C:7]1[NH:8][CH:9]=[CH:10][N:11]=1)([CH3:3])[CH3:2]

Participants

4

Reactant 3

HCID 6909Trichloroisocyanuric AcidHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 58951908HCID 58951908, compound

Product 1

HCID 58951824HCID 58951824, compound

Procedure

2-(2,6-Diisopropyl-benzyl)-1H-imidazole was prepared from 2-(2,6-diisopropyl-benzyl)-4,5-dihydro-1H-imidazole (Example 4), TCCA and DBU in analogy to Example 194e): yellow crystals; MS (ISP): 243.4 ([M+H]+).

Sources & evidence

ORD record
ord-951bd66296824c0f8af8e7958930c890
Source dataset
uspto-grants-2011_01
Patent number
US07875645B2

Reaction notes

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