2-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one → HCID 9886615, compound

HRID 1596420Notes

Reaction equation

HRID 1596420 reaction equation
[Br:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:11])[CH:8]=2)[C:3]1=[O:12].[CH:13]1([C:19](=[S:21])[NH2:20])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>>[BrH:1].[Cl:11][C:7]1[CH:6]=[CH:5][C:4]2[C:3]3([OH:12])[N:20]=[C:19]([CH:13]4[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]4)[S:21][CH:2]3[CH2:10][C:9]=2[CH:8]=1

Participants

3

Reactant 2

HCID 113340692-Bromo-5-chloro-2,3-dihydro-1H-inden-1-oneHCID 12336049Cyclohexanecarbothioamide

Product 1

HCID 9886615HCID 9886615, compound

Procedure

This compound is prepared analogously to the process described in Example 1c using 2-bromo-5-chloroindan-1-one and cyclohexanethiocarboxamide; melting point: 170-175° C. (dec.).

Workup

  1. customThis compound is prepared analogously to the process

Sources & evidence

ORD record
ord-fe0012462e694a6ab6ea956ca24c23f5
Source dataset
uspto-grants-2001_09
Patent number
US06291486B1

Reaction notes

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