(R)-(-)-1-Aminoindan → HCID 67095932, compound

HRID 2076316Notes

Reaction equation

HRID 2076316 reaction equation
[I:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[NH2:13][C@H:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15]1>>[C@H:14]1([NH:13][C:6]2[CH:5]=[CH:4][C:3]3[C:8](=[CH:9][CH:10]=[CH:11][C:2]=3[I:1])[N:7]=2)[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16][CH2:15]1

Participants

3

Reactant 2

HCID 2733933(R)-(-)-1-AminoindanHCID 457894242-Chloro-5-iodoquinoline

Product 1

HCID 67095932HCID 67095932, compound

Procedure

(R)-Indan-1-yl-(5-iodo-quinolin-2-yl)-amine was prepared from 5-iodo-2-chloroquinoline and (R)-1-aminoindane as described in example 6 step A.

Sources & evidence

ORD record
ord-b8559766fdd44ea3825f3fe6391d6af6
Source dataset
uspto-grants-2011_04
Patent number
US07923561B2

Reaction notes

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