HCID 67514156, compound → HCID 86694488, compound

HRID 1519647Notes

Reaction equation

HRID 1519647 reaction equation
[O:1]=[C:2]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][CH:12]=O)=[CH:10][C:5]=2[CH2:4][O:3]1.[N:14]1([CH:20]2[CH2:29][CH2:28][C:27]3[CH:26]=[C:25]([C:30]#[N:31])[CH:24]=[CH:23][C:22]=3[CH2:21]2)[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1>>[O:1]=[C:2]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][CH2:12][N:17]3[CH2:16][CH2:15][N:14]([CH:20]4[CH2:29][CH2:28][C:27]5[CH:26]=[C:25]([C:30]#[N:31])[CH:24]=[CH:23][C:22]=5[CH2:21]4)[CH2:19][CH2:18]3)=[CH:10][C:5]=2[CH2:4][O:3]1

Participants

3

Reactant 2

HCID 67514156HCID 67514156, compoundHCID 772312612-(1-Oxo-1,3-dihydroisobenzofuran-5-yl)acetaldehyde

Product 1

HCID 86694488HCID 86694488, compound

Procedure

The above product was prepared following similar procedure of EXAMPLE 38 from (1-oxo-1,3-dihydro-2-benzofuran-5-yl)acetaldehyde and 6-piperazin-1-yl-5,6,7,8-tetrahydronaphthalene-2-carbonitrile. LC-MS (IE, m/z): 402 [M+1]+. (0.050 μM)

Workup

  1. customThe above product was prepared

Sources & evidence

ORD record
ord-e470676b8b4a4309986054200c9a409d
Source dataset
uspto-grants-2015_07
Patent number
US09073882B2

Reaction notes

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