HCID 10220223, compound → HCID 9882375, compound
Reaction equation
NC1SC2C3C(CC=2C=1[C:14]([NH2:16])=[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:31]([NH2:33])=[O:32])=[CH:27][CH:26]=[CH:25][CH:24]=3>>[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:31]([NH2:33])=[O:32])=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:14]([NH2:16])=[O:15]Participants
3
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-4,5-dihydro-naphtho[1,2-b]thiophene-3-carboxylic acid amide to give the above title compound as brown solid. ESMS m/z: 288 [M+H]+.
Sources & evidence
- ORD record
- ord-575b0945acd741a69042c8ecc32e5017
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183311B2
Reaction notes
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