Methyl 4-(Chlorosulfonyl)benzoate → HCID 66837921, compound

HRID 73123Notes

Reaction equation

HRID 73123 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].[N:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[C:17]([CH2:25][NH2:26])[CH:16]=1>>[N:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[C:17]([CH2:25][NH:26][S:2]([C:5]2[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][CH:6]=2)(=[O:4])=[O:3])[CH:16]=1

Participants

3

Reactant 2

HCID 4738388Methyl 4-(Chlorosulfonyl)benzoateHCID 6483745Quinolin-3-ylmethanamine

Product 1

HCID 66837921HCID 66837921, compound

Procedure

The titled compound was prepared according to the procedure described in step-1 of Example 1 from methyl 4-(chlorosulfonyl)benzoate and quinolin-3-ylmethanamine.

Sources & evidence

ORD record
ord-e43464352d574edea2b2b2068d527fa7
Source dataset
uspto-grants-2014_09
Patent number
US08829026B2

Reaction notes

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