HCID 10220223, compound → HCID 10406561, compound

HRID 351116Notes

Reaction equation

HRID 351116 reaction equation
NC1SC2C3C(CC=2C=1[C:14]([NH2:16])=[O:15])=CC=CC=3.FC(F)(F)C(O)=O.[NH2:24][C:25]1[S:29][C:28]2[C:30]3[C:35]([CH2:36][CH2:37][C:27]=2[C:26]=1[C:39]([NH2:41])=[O:40])=[CH:34][C:33]([Br:38])=[CH:32][CH:31]=3>>[Br:38][C:33]1[CH:34]=[C:35]2[C:30](=[CH:31][CH:32]=1)[C:28]1[S:29][C:25]([NH:24][C:14]([NH2:16])=[O:15])=[C:26]([C:39]([NH2:41])=[O:40])[C:27]=1[CH2:37][CH2:36]2

Participants

3

Reactant 2

HCID 10220223HCID 10220223, compoundHCID 69370131HCID 69370131, compound

Product 1

HCID 10406561HCID 10406561, compound

Procedure

The title compound was prepared by the same procedure as Example 2 except 2-amino-4H-indeno[1,2-b]thiophene-3-carboxylic acid amide was replaced with 2-amino-7-bromo-4,5-dihydro-naphtho[1,2-b]thiophene-3-carboxylic acid amide trifluoroacetate to give the above title compound as brown solid. ESMS m/z: 367 [M+H]+.

Sources & evidence

ORD record
ord-74a6f9c1a7264989927c6c500208965e
Source dataset
uspto-grants-2007_02
Patent number
US07183311B2

Reaction notes

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