4-Methoxybenzenesulfonyl chloride → HCID 54050438, compound

HRID 1141498Notes

Reaction equation

HRID 1141498 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][O:8][c:9]1[cH:10][c:11]([CH2:15][NH:16][CH2:17][c:18]2[cH:19][cH:20][c:21](-[n:24]3[n:25][cH:26][cH:27][cH:28]3)[cH:22][cH:23]2)[cH:12][cH:13][cH:14]1)=[O:29].[CH3:30][O:31][c:32]1[cH:33][cH:34][c:35]([S:38](=[O:39])(=[O:40])[Cl:41])[cH:36][cH:37]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH2:7][O:8][c:9]1[cH:10][c:11]([CH2:15][N:16]([CH2:17][c:18]2[cH:19][cH:20][c:21](-[n:24]3[n:25][cH:26][cH:27][cH:28]3)[cH:22][cH:23]2)[S:38]([c:35]2[cH:34][cH:33][c:32]([O:31][CH3:30])[cH:37][cH:36]2)(=[O:39])=[O:40])[cH:12][cH:13][cH:14]1)=[O:29]

Participants

3

Reactant 2

HCID 74014-Methoxybenzenesulfonyl chlorideHCID 54338479{3-[(4-Pyrazol-1-yl-benzylamino)-methyl]-phenoxy}-acetic acid tert-butyl ester

Product 1

HCID 54050438HCID 54050438, compound

Sources & evidence

ORD record
ord-aa29ecdf15664d6695e2de6159accf9b
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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