(+-)-1-Aminoindan → HCID 51273555, compound

HRID 1967501Notes

Reaction equation

HRID 1967501 reaction equation
[N:1]1([S:7]([C:10]2[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=2)[C:13]([OH:15])=O)(=[O:9])=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[NH2:19][CH:20]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH2:22][CH2:21]1>>[CH:20]1([NH:19][C:13](=[O:15])[C:12]2[CH:16]=[CH:17][CH:18]=[C:10]([S:7]([N:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)(=[O:8])=[O:9])[CH:11]=2)[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH2:22][CH2:21]1

Participants

3

Reactant 2

HCID 123445(+-)-1-AminoindanHCID 7678893-(Piperidine-1-sulfonyl)benzoic acid

Product 1

HCID 51273555HCID 51273555, compound

Procedure

The entitled compound was produced according to the method of Example 73 but using 3-(piperidin-1-ylsulfonyl)benzoic acid and 1-aminoindane as the starting materials.

Workup

  1. customThe entitled compound was produced

Sources & evidence

ORD record
ord-434c15eddd07417bb2374691e39ba8ff
Source dataset
uspto-grants-2013_04
Patent number
US08420823B2

Reaction notes

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