4-methyl-5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one hydrochloride → 4-Methyl-5-[2-[4-[2-[6-(tetrazol-1-yl)-3-pyridyl)ethyl]piperazin-1-yl]ethyl]-3H-isobenzofuran-1-one
Reaction equation
Cl.[CH3:2][C:3]1[C:11]2[CH2:10][O:9][C:8](=[O:12])[C:7]=2[CH:6]=[CH:5][C:4]=1[CH2:13][CH2:14][N:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1.[N:21]1([C:26]2[N:31]=[CH:30][C:29]([CH2:32][CH:33]=O)=[CH:28][CH:27]=2)[CH:25]=[N:24][N:23]=[N:22]1>>[CH3:2][C:3]1[C:4]([CH2:13][CH2:14][N:15]2[CH2:20][CH2:19][N:18]([CH2:33][CH2:32][C:29]3[CH:30]=[N:31][C:26]([N:21]4[CH:25]=[N:24][N:23]=[N:22]4)=[CH:27][CH:28]=3)[CH2:17][CH2:16]2)=[CH:5][CH:6]=[C:7]2[C:11]=1[CH2:10][O:9][C:8]2=[O:12]Participants
3
Procedure
4-Methyl-5-[2-[4-[2-[6-(tetrazol-1-yl)-3-pyridyl]ethyl]piperazin-1-yl]ethyl]-3H-isobenzofuran-1-one was prepared in a similar fashion to that described for the synthesis of Example 38 starting from 4-methyl-5-[2-(piperazin-1-yl)ethyl]-2-benzofuran-1(3H)-one hydrochloride and [6-(1H-tetrazol-1-yl)pyridin-3-yl]acetaldehyde. LC-MS (IE, m/z): 406.1 [(M+1)+−28]. (0.61 μm)
Sources & evidence
- ORD record
- ord-d1e68d26cc254a1dba350084f73341fc
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09073882B2
Reaction notes
Loading…