HCID 10220223, compound → HCID 10425891, compound

HRID 351114Notes

Reaction equation

HRID 351114 reaction equation
NC1SC2C3C(CC=2[C:3]=1[C:14](N)=[O:15])=CC=CC=3.[NH2:17][C:18]1[S:22][C:21]2[C:23]3[C:28]([CH2:29][CH2:30][C:20]=2[C:19]=1[C:33]([NH2:35])=[O:34])=[CH:27][C:26]([O:31][CH3:32])=[CH:25][CH:24]=3>>[C:14]([NH:17][C:18]1[S:22][C:21]2[C:23]3[C:28]([CH2:29][CH2:30][C:20]=2[C:19]=1[C:33]([NH2:35])=[O:34])=[CH:27][C:26]([O:31][CH3:32])=[CH:25][CH:24]=3)(=[O:15])[CH3:3]

Participants

3

Reactant 2

HCID 10220223HCID 10220223, compoundHCID 10446032HCID 10446032, compound

Product 1

HCID 10425891HCID 10425891, compound

Procedure

The title compound was prepared by the same procedure as Example 3 except that 2-amino-4H-indeno[1,2-b]thiophene-3-carboxylic acid amide was replaced with 2-amino-7-methoxy-4,5-dihydro-naphtho[1,2-b]thiophene-3-carboxylic acid amide to give the above title compound as light grey solid. ESMS m/z: 317 [M+H]+.

Sources & evidence

ORD record
ord-3fa19e0c4e3f43838a22fe09456f1b1e
Source dataset
uspto-grants-2007_02
Patent number
US07183311B2

Reaction notes

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