R-56109 hydrochloride → HCID 21471892, compound
Reaction equation
[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[S:10][C:11]([CH3:16])=[C:12]([CH2:13][CH2:14]Cl)[C:6]=2[CH2:5]1)(=[O:3])[CH3:2].Cl.[F:18][C:19]1[CH:33]=[CH:32][C:22]2[C:23]([CH:26]3[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]3)=[N:24][O:25][C:21]=2[CH:20]=1>>[C:1]([N:4]1[CH2:9][CH2:8][C:7]2[S:10][C:11]([CH3:16])=[C:12]([CH2:13][CH2:14][N:29]3[CH2:28][CH2:27][CH:26]([C:23]4[C:22]5[CH:32]=[CH:33][C:19]([F:18])=[CH:20][C:21]=5[O:25][N:24]=4)[CH2:31][CH2:30]3)[C:6]=2[CH2:5]1)(=[O:3])[CH3:2]Participants
3
Procedure
The reaction and procedure were conducted in a similar manner as in Example 24 using 2.0 g of 5-acetyl-3-(2-chloroethyl)-4,5,6,7-tetrahydro-2-methylthieno[3,2-c]pyridine and 1.0 g of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine hydrochloride to give 0.25 g of 5-acetyl-3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[3,2-c]pyridine as an oil.
Workup
- customThe reaction and procedure
Sources & evidence
- ORD record
- ord-cf88303a29f04ff68394ec72a76595b5
- Source dataset
- uspto-grants-1996_07
- Patent number
- US05532240
Reaction notes
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