Bromoacetyl bromide → HCID 22251579, compound

HRID 1098098Notes

Reaction equation

[Br:1][CH2:2][C:3](Br)=[O:4].[NH2:6][C:7]1[S:8][CH:9]=[C:10]([CH3:12])[N:11]=1>>[Br:1][CH2:2][C:3]([NH:6][C:7]1[S:8][CH:9]=[C:10]([CH3:12])[N:11]=1)=[O:4]

Participants

Reactant 2

HCID 61147Bromoacetyl bromide

HCID 741432-Amino-4-methylthiazole

Product 1

HCID 22251579HCID 22251579, compound

Procedure

The title compound was prepared in a manner similar to that described for Intermediate A16 (Step 5) starting from bromoacetyl bromide and 2-amino-4-methylthiazole.

Sources & evidence

ORD record: ord-4386568f28f94b28aa780561adb14766
Source dataset: uspto-grants-2012_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08143263B2

Reaction notes

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