HCID 59054439, compound → HCID 59054440, compound

HRID 1400269Notes

Reaction equation

HRID 1400269 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[S:12]([CH2:15][CH2:16][NH:17][CH2:18][C:19]1[O:20][CH:21]=[CH:22][CH:23]=1)(=[O:14])=[O:13].Cl[C:25]1C2C(=CC=CC=2)C=CC=1SCCNCC1OC(C)=CC=1>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[S:12]([CH2:15][CH2:16][NH:17][CH2:18][C:19]1[O:20][C:21]([CH3:25])=[CH:22][CH:23]=1)(=[O:14])=[O:13]

Participants

3

Reactant 2

HCID 59054439HCID 59054439, compoundHCID 68151593HCID 68151593, compound

Product 1

HCID 59054440HCID 59054440, compoundYield 59%

Procedure

Prepared as described for compound 25, from 2-[(1-chloronaphthalen-2-yl)sulfanyl]-N-[(5-methylfuran-2-yl)methyl]ethanamine in 59% yield as white solid.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-df73f7995d454b52a7601d64dbe61303
Source dataset
uspto-grants-2014_12
Patent number
US08906946B2

Reaction notes

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