1-(Morpholinocarbonylmethyl)piperazine → HCID 69459604, compound
Reaction equation
C(C1C=CC(C2N(C(Cl)=O)[C@H](C3C=CC(Cl)=CC=3)[C@H](C3C=CC([Cl:22])=CC=3)N=2)=C(OCC(F)(F)F)C=1)(C)(C)C.[N:39]1([C:45](=[O:53])[CH2:46]N2CCNCC2)[CH2:44][CH2:43][O:42][CH2:41][CH2:40]1>>[ClH:22].[N:39]1([C:45](=[O:53])[CH3:46])[CH2:44][CH2:43][O:42][CH2:41][CH2:40]1Participants
3
Procedure
(4S,5R)-2-[4-tert-butyl-2-(2,2,2-trifluoro-ethoxy)-phenyl]-4,5-bis-(4-chloro-phenyl)-4,5-dihydro-imidazole-1-carbonyl]-piperazin-1-yl}-1-morpholin-4-yl-ethanone hydrochloride was prepared from (4S,5R)-2-[4-tert-butyl-2-(2,2,2-trifluoro-ethoxy)-phenyl]-4,5-bis-(4-chloro-phenyl)-4,5-dihydro-imidazole-1-carbonyl chloride (example 12l) and 1-morpholin-4-yl-2-piperazin-1-yl-ethanone (Oakwood Products) in an analogous manner as described in example 25. LR-MS: 760.5 [(M+H)+]
Sources & evidence
- ORD record
- ord-fdcc76a288f649f18f51c1435a0b5fb9
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964724B2
Reaction notes
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