HCID 43581407, compound → HCID 44219027, compound
Reaction equation
[O:1]=[S:2]1(=[O:12])[CH2:7][CH2:6][N:5]([S:8](Cl)(=[O:10])=[O:9])[CH2:4][CH2:3]1.[C@H:13]1([NH:22][C:23]2[CH:32]=[CH:31][C:30]3[C:25](=[CH:26][CH:27]=[C:28]([NH2:33])[CH:29]=3)[N:24]=2)[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:15][CH2:14]1>>[C@H:13]1([NH:22][C:23]2[CH:32]=[CH:31][C:30]3[C:25](=[CH:26][CH:27]=[C:28]([NH:33][S:8]([N:5]4[CH2:6][CH2:7][S:2](=[O:12])(=[O:1])[CH2:3][CH2:4]4)(=[O:10])=[O:9])[CH:29]=3)[N:24]=2)[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:15][CH2:14]1Participants
3
Procedure
The title compound was prepared in accordance with the general method described in example 66 from 1,1-dioxo-thiomorpholine-4-sulfonyl chloride and (R)—N2-indan-1-yl-quinoline-2,6-diamine; MS: m/e=473.7 (M+H+).
Sources & evidence
- ORD record
- ord-40d1aebc75914e1ba53f10d1e0bbf2ca
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08183380B2
Reaction notes
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