HCID 25069604, compound → HCID 68597377, compound

HRID 1890373Notes

Reaction equation

HRID 1890373 reaction equation
[O:1]1[C:5]([C:6]2[CH:11]=[CH:10][C:9]([S:12]([N:15]3[C:23]4[C:18](=[CH:19][C:20]([CH:24]5[CH2:27][N:26]([CH2:28][CH2:29][CH3:30])[CH2:25]5)=[CH:21][CH:22]=4)[CH:17]=[CH:16]3)(=[O:14])=[O:13])=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1.[ClH:31].C1(S(N2C3C(=CC(C4CN(CCC)C4)=CC=3)CC2)(=O)=O)C=CC=CC=1>>[ClH:31].[O:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([S:12]([N:15]3[C:23]4[C:18](=[CH:19][C:20]([CH:24]5[CH2:27][N:26]([CH2:28][CH2:29][CH3:30])[CH2:25]5)=[CH:21][CH:22]=4)[CH2:17][CH2:16]3)(=[O:14])=[O:13])=[CH:10][CH:11]=2)=[CH:4][N:3]=[CH:2]1

Participants

3

Reactant 2

HCID 25069604HCID 25069604, compoundHCID 68595934HCID 68595934, compound

Product 1

HCID 68597377HCID 68597377, compound

Procedure

This compound was prepared from 1-(4-oxazol-5-yl-benzensulfonyl)-5-(1-propyl-azetidin-3-yl)-1H-indole by the method outlined for compound 9. ESI-MS [m/z]: 424.15 [M+H]+.

Sources & evidence

ORD record
ord-b4078cb9c25e4880bf26bd8043165f78
Source dataset
uspto-grants-2013_08
Patent number
US08507469B2

Reaction notes

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