2-Thiazolesulfonyl chloride → HCID 54506282, compound

HRID 2155469Notes

Reaction equation

HRID 2155469 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].[s:30]1[c:31]([S:35](=[O:36])(=[O:37])[Cl:38])[n:32][cH:33][cH:34]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:35]([c:31]2[s:30][cH:34][cH:33][n:32]2)(=[O:36])=[O:37])[cH:12][cH:13][cH:14]1)=[O:29]

Participants

3

Reactant 2

HCID 115792352-Thiazolesulfonyl chlorideHCID 54338479{3-[(4-Pyrazol-1-yl-benzylamino)-methyl]-phenoxy}-acetic acid tert-butyl ester

Product 1

HCID 54506282HCID 54506282, compound

Sources & evidence

ORD record
ord-1238aa82029f4967a93ddea8c2f94b98
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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