2-Aminoindane → HCID 67095942, compound

HRID 2076288Notes

Reaction equation

HRID 2076288 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[F:15][C:16]1[CH:17]=[C:18]([S:24](Cl)(=[O:26])=[O:25])[CH:19]=[C:20]([F:23])[C:21]=1[F:22].[NH2:28][CH:29]1[CH2:37][C:36]2[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=2)[CH2:30]1>>[F:15][C:16]1[CH:17]=[C:18]([S:24]([NH:1][C:4]2[CH:13]=[CH:12][CH:11]=[C:10]3[C:5]=2[CH:6]=[CH:7][C:8]([NH:28][CH:29]2[CH2:37][C:36]4[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=4)[CH2:30]2)=[N:9]3)(=[O:26])=[O:25])[CH:19]=[C:20]([F:23])[C:21]=1[F:22]

Participants

4

Reactant 3

HCID 763102-AminoindaneHCID 3192512-Chloro-5-nitroquinolineHCID 27788583,4,5-Trifluorobenzenesulfonyl chloride

Product 1

HCID 67095942HCID 67095942, compound

Procedure

The title compound, MS: m/e=470.5 (M+H+), was prepared in accordance with the general method of example 13 from 5-nitro-2-chloroquinoline, 3,4,5-trifluorobenzenesulfonyl chloride and 2-aminoindane.

Sources & evidence

ORD record
ord-f29af1b1d06b4b71a3711a746797eeae
Source dataset
uspto-grants-2011_04
Patent number
US07923561B2

Reaction notes

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