HCID 67344581, compound → HCID 67345624, compound

HRID 1670027Notes

Reaction equation

HRID 1670027 reaction equation
N1CC[C@H](N(C2CCCCC2)CC(OC)=O)[CH2:2]1.[C:18]([N:25]1[CH2:30][CH2:29][CH:28]([N:31]([CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)[C:32](=[O:37])[NH:33][CH:34]([CH3:36])[CH3:35])[CH2:27][CH2:26]1)([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19]>>[C:18]([N:25]1[CH2:30][CH2:29][CH:28]([N:31]([CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)[C:32](=[O:37])[N:33]([CH3:2])[CH:34]([CH3:35])[CH3:36])[CH2:27][CH2:26]1)([O:20][C:21]([CH3:22])([CH3:23])[CH3:24])=[O:19]

Participants

3

Reactant 2

HCID 67344581HCID 67344581, compoundHCID 67346737HCID 67346737, compound

Product 1

HCID 67345624HCID 67345624, compound

Procedure

The title compound was prepared following the procedure described in Step A of Intermediate 128 using 1-BOC-4-[cyclohexyl(isopropylcarbamoyl)amino]piperidine.

Sources & evidence

ORD record
ord-8a92b987ee3f42a4847ac49fb508ffee
Source dataset
uspto-grants-2011_08
Patent number
US07989634B2

Reaction notes

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