Benzyl Bromide → HCID 57422337, compound

HRID 2094895Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[C:5]([O:11][CH3:12])[C:4]=1[CH2:13][NH2:14].Cl[S:16]([C:19]1[CH:28]=[CH:27][C:22]([C:23]([O:25]C)=[O:24])=[CH:21][CH:20]=1)(=[O:18])=[O:17].[CH2:29](Br)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[CH2:29]([N:14]([CH2:13][C:4]1[C:5]([O:11][CH3:12])=[CH:6][C:7]([O:9][CH3:10])=[CH:8][C:3]=1[O:2][CH3:1])[S:16]([C:19]1[CH:28]=[CH:27][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=1)(=[O:18])=[O:17])[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1

Participants

Reactant 3

HCID 7498Benzyl Bromide

HCID 688109(2,4,6-Trimethoxyphenyl)methanamine

HCID 4738388Methyl 4-(Chlorosulfonyl)benzoate

Product 1

HCID 57422337HCID 57422337, compound

Procedure

Prepared as in example 5-10 from (2,4,6-trimethoxyphenyl)methanamine, methyl 4-(chlorosulfonyl)benzoate (Example 5-10c) and benzyl bromide. MS (M−H, 470.10); 1H NMR (400 MHz, DMSO-d6): δ, ppm: 3.45(s, 6H), 3.69(s, 3H), 4.26(s, 2H), 4.28(s, 2H), 5.98(s, 2H), 7.11-7.26(m, 5H), 7.82(d, J=8.0 Hz, 2H), 8.07(d, J=8 Hz, 2H), 13.49(s, 1H). Elemental analysis (found, %): C, 61.05; H, 5.49; N, 2.98; (calculated, %): C, 61.13; H, 5.34 and N, 2.97.

Sources & evidence

ORD record: ord-3bb4a545d96c4df3a40d54ea361307a6
Source dataset: uspto-grants-2013_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08445692B2

Reaction notes

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