HCID 817251, compound → HCID 86653057, compound

HRID 1951208Notes

Reaction equation

HRID 1951208 reaction equation
[CH3:1]C1N=C(C)C=C(C)N=1.[Br:10][CH:11]([C:15]1[CH:20]=[C:19]([CH3:21])[N:18]=[C:17](SC)[N:16]=1)[C:12](=[O:14])[CH3:13].CC1C=C(C)N=C(SC)N=1>>[Br:10][CH:11]([C:15]1[CH:20]=[C:19]([CH3:21])[N:18]=[C:17]([CH3:1])[N:16]=1)[C:12](=[O:14])[CH3:13]

Participants

4

Reactant 3

HCID 817251HCID 817251, compoundHCID 123431744,6-Dimethyl-2-(methylsulfanyl)pyrimidineHCID 86653056HCID 86653056, compound

Product 1

HCID 86653057HCID 86653057, compound

Procedure

This material is prepared from 2,4,6-trimethyl-pyrimidine following the 2-step protocol used to prepare 1-bromo-1-(6-methyl-2-methylsulfanyl-pyrimidin-4-yl)-propan-2-one (AC3) from 4,6-dimethyl-2-methylsulfanyl-pyrimidine (AC1).

Sources & evidence

ORD record
ord-568dd72dd32f48b19ace04552962d4f6
Source dataset
uspto-grants-2013_03
Patent number
US08404684B2

Reaction notes

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