HCID 59054439, compound → HCID 59053462, compound

HRID 1400271Notes

Reaction equation

HRID 1400271 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]1O[CH:21]=[CH:22][CH:23]=1)(=[O:14])=[O:13].ClC1C2C(=CC=CC=2)C=CC=1[S:35]CCNCC1SC=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[S:35][CH:21]=[CH:22][CH:23]=1)(=[O:14])=[O:13]

Participants

3

Procedure

Prepared as described for compound 25 from 2-[(1-chloronaphthalen-2-yl)sulfanyl]-N-(thiophen-2-ylmethyl)ethanamine in 68% yield as yellow solid.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-5f9e1532e01a4bb18d3f3447b2a047bc
Source dataset
uspto-grants-2014_12
Patent number
US08906946B2

Reaction notes

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