Bromoacetonitrile → HCID 86641788, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([N:7]2[CH2:12][CH2:11][O:10][CH2:9][CH2:8]2)[CH2:3][CH2:2]1.Br[CH2:14][C:15]#[N:16]>>[N:7]1([CH:4]2[CH2:5][CH2:6][N:1]([CH2:14][C:15]#[N:16])[CH2:2][CH2:3]2)[CH2:12][CH2:11][O:10][CH2:9][CH2:8]1Participants
3
Procedure
The title compound is synthesized by coupling of 4-Piperidin-4-yl-morpholine (commercially available from CHESS GmbH) and bromoacetonitrile analogously to the preparation of Intermediate 149.2 as a colorless oil; ES-MS: M+=210.1: 1HNMR(DMSO-d6) 3.65 (s, 2H), 3.55 (t, 4H), 2.80-2.75 (m, 2H), 2.40 (t, 4H), 2.15-2.00 (m, 3H), 1.80-1.70 (m, 2H), 1.40-1.30 (m, 2H).
Workup
- customanalogously to the preparation of Intermediate 149.2 as a colorless oil
Sources & evidence
- ORD record
- ord-3096b66636b5464b9b6db85fb81da4ab
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08053457B2
Reaction notes
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