(1-Methyl-1H-1,2,3-Benzotriazol-5-Yl)Methylamine → HCID 66837875, compound

Reaction equation

Cl[S:2]([C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[CH3:15][N:16]1[C:20]2[CH:21]=[CH:22][C:23]([CH2:25][NH2:26])=[CH:24][C:19]=2[N:18]=[N:17]1>>[CH3:15][N:16]1[C:20]2[CH:21]=[CH:22][C:23]([CH2:25][NH:26][S:2]([C:5]3[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=3)(=[O:4])=[O:3])=[CH:24][C:19]=2[N:18]=[N:17]1

Participants

Reactant 2

HCID 2795420(1-Methyl-1H-1,2,3-Benzotriazol-5-Yl)Methylamine

HCID 4738388Methyl 4-(Chlorosulfonyl)benzoate

Product 1

HCID 66837875HCID 66837875, compound

Procedure

The titled compound was prepared according to the procedure described in step-1 of Example 1 from methyl 4-(chlorosulfonyl)benzoate and (1-methyl-1H-benzo[d][1,2,3]triazol-5-yl)methanamine.

Sources & evidence

ORD record: ord-632245b0e67f4f6496d303625fc283a0
Source dataset: uspto-grants-2014_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08829026B2

Reaction notes

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