4-Methylmorpholine → HCID 86611238, compound

HRID 734327Notes

Reaction equation

HRID 734327 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:14][CH2:13][CH:12]([C:15]([OH:17])=O)[CH2:11][CH2:10]2)=[CH:5][CH:4]=1)#[N:2].Cl.Cl.[CH3:20][C@H:21]1[CH2:26][NH:25][CH2:24][C@H:23]([CH3:27])[NH:22]1.C1C=CC2N(O)N=NC=2C=1.CN1CCOCC1>CN(C=O)C.C(Cl)CCl>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH2:10][CH2:11][CH:12]([C:15]([N:25]3[CH2:24][C@H:23]([CH3:27])[NH:22][C@@H:21]([CH3:20])[CH2:26]3)=[O:17])[CH2:13][CH2:14]2)=[CH:7][CH:8]=1)#[N:2]

Participants

7

Procedure

The title compound (D18) was prepared using a similar procedure to Description 4 step 1from 1-(4-cyanophenyl)-piperidine4-carboxylic acid (D3), (2S, 6S)-2,6-dimethylpiperazine dihydrochloride (J. W. Mickleson, K. L. Belonga and E. J. Jacobsen, J. Org. Chem., 1995, 60(13), 4177-4183), EDC, HOBT and N-methyl morpholine in DMF.

Sources & evidence

ORD record
ord-6885547383de410c91f2bea68a58a80c
Source dataset
uspto-grants-2009_09
Patent number
US07592347B2

Reaction notes

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