2-Bromothiazole → HCID 178455566, compound

HRID 137913Notes

Reaction equation

HRID 137913 reaction equation
[Br:1][c:2]1[s:3][cH:4][cH:5][n:6]1.[C:12]([CH3:13])([CH3:14])([CH3:15])[Si:16]([O:17][CH:18]([CH:19]=[N:20][S:21](=[O:22])[C:23]([CH3:24])([CH3:25])[CH3:26])[CH2:27][O:28][Si:29]([CH3:30])([CH3:31])[C:32]([CH3:33])([CH3:34])[CH3:35])([CH3:36])[CH3:37].[CH2:7]([Li:8])[CH2:9][CH2:10][CH3:11]>>[c:2]1([CH:19]([CH:18]([O:17][Si:16]([C:12]([CH3:13])([CH3:14])[CH3:15])([CH3:36])[CH3:37])[CH2:27][O:28][Si:29]([CH3:30])([CH3:31])[C:32]([CH3:33])([CH3:34])[CH3:35])[NH:20][S:21](=[O:22])[C:23]([CH3:24])([CH3:25])[CH3:26])[s:3][cH:4][cH:5][n:6]1

Participants

4

Reactant 3

HCID 764302-BromothiazoleHCID 74961661N-[2,3-bis[[tert-butyl(dimethyl)silyl]oxy]propylidene]-2-methylpropane-2-sulfinamideHCID 178418339Butyllithium

Product 1

HCID 178455566HCID 178455566, compound

Sources & evidence

ORD record
ord-67f82fb928df45ffb95edc9c97e38307
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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