HCID 19846145, compound → HCID 19846138, compound
Reaction equation
Cl.[NH2:2][CH2:3][C:4]([NH:6][C:7]1([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2Br)[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:8]1)=[O:5].Cl.N[CH2:25][C:26](NC1(C2C=CC(Cl)=CC=2)CC2C(=CC=CC=2)C1)=[O:27].Cl.N[CH2:47][C:48](NC1(C2C=CC=C(C)C=2)CC2C(=CC=CC=2)C1)=O.Cl.NCC(NC1(C2C=CC(C(F)(F)F)=CC=2)CC2C(=CC=CC=2)C1)=O.Cl.NCC(NC1(C2C=CC=C(F)C=2)CC2C(=CC=CC=2)C1)=O.Cl.NCC(NC1(C2C=CC(OC)=CC=2)CC2C(=CC=CC=2)C1)=O.Cl.NCC(NC1(C2C=CC(OC)=C(OC)C=2)CC2C(=CC=CC=2)C1)=O.Cl.NCC(NC1(C2C=CC(F)=CC=2F)CC2C(=CC=CC=2)C1)=O.Cl.CNCC(NC1(C2C=CC(OCCCC)=CC=2)CC2C(=CC=CC=2)C1)=O.Cl.CN(C)CC(NC1(C2C=CC(CCCC)=CC=2)CC2C(=CC=CC=2)C1)=O>>[C:16]1([C:7]2([NH:6][C:4](=[O:5])[CH2:3][N:2]3[CH2:25][CH2:26][O:27][CH2:48][CH2:47]3)[CH2:15][C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[CH2:8]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Participants
Reactant 10
Product 1
Procedure
Application of the methodology described above will provide all the compounds of the invention including, for example, the following compounds: 2-amino-N-[2,3-dihydro-2(2-bromophenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(4-chlorophenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(3-methylphenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-[4-(trifluoromethyl)phenyl]-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(3-fluorophenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(4-methoxyphenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(3,4-dimethoxyphenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-amino-N-[2,3-dihydro-2-(2,4-difluoro-phenyl)-1H-inden-2-yl]acetamide hydrochloride; 2-(methyl-amino)-N-[2,3-dihydro-2-(4-n-butoxyphenyl)-1H-inden-2yl]acetamide hydrochloride; 2-(dimethylamino)-N-[2,3-dihydro-2-(4-n-butylphenyl)-1H-inden-2-yl]acetamide hydrochloride.
Workup
- customApplication of the methodology described above will provide all the compounds of the invention
Sources & evidence
- ORD record
- ord-cd7a6722a345489aabd4d728121eabb9
- Source dataset
- uspto-grants-1989_10
- Patent number
- US04873241
Reaction notes
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