Benzyl Bromide → HCID 25205356, compound

HRID 2094893Notes

Reaction equation

HRID 2094893 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[CH:5][C:4]=1[CH2:11][NH2:12].Cl[S:14]([C:17]1[CH:26]=[CH:25][C:20]([C:21]([O:23]C)=[O:22])=[CH:19][CH:18]=1)(=[O:16])=[O:15].[CH2:27](Br)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH2:27]([N:12]([CH2:11][C:4]1[CH:5]=[CH:6][C:7]([O:9][CH3:10])=[CH:8][C:3]=1[O:2][CH3:1])[S:14]([C:17]1[CH:26]=[CH:25][C:20]([C:21]([OH:23])=[O:22])=[CH:19][CH:18]=1)(=[O:16])=[O:15])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1

Participants

4

Reactant 3

HCID 7498Benzyl BromideHCID 5972502,4-DimethoxybenzylamineHCID 4738388Methyl 4-(Chlorosulfonyl)benzoate

Product 1

HCID 25205356HCID 25205356, compound

Procedure

Prepared as in example 5-10 from (2,4-dimethoxyphenyl)methanamine, methyl 4-(chlorosulfonyl)benzoate (Example 5-10c) and benzyl bromide. MS (M−H, 440.10); 1H NMR (400 MHz, DMSO-d6): δ, ppm: 3.50(s, 63H), 3.66(s, 3H), 4.20(s, 2H), 4.34(s, 2H), 6.29(s, 1H), 6.33(d, J=8.0 Hz, 1H), 6.91(d, J=8.8 Hz, 1H), 7.12-7.23 (m, 5H), 7.80(d, J=8.0 Hz, 2H), 8.01 (d, J=8.4 Hz, 2H), 13.49(s, 1H).

Sources & evidence

ORD record
ord-6be8115b7a4a40d0b458ee9d8cfda1ca
Source dataset
uspto-grants-2013_05
Patent number
US08445692B2

Reaction notes

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