HCID 22256535, compound → HCID 22256527, compound

HRID 1611254Notes

Reaction equation

HRID 1611254 reaction equation
C([O:8][N:9]([CH2:12][CH:13]([CH2:17][CH2:18][CH2:19][CH3:20])[C:14]([OH:16])=O)[CH:10]=[O:11])C1C=CC=CC=1.[NH:21]1[CH2:25][CH2:24][CH2:23][C@H:22]1[C:26]1[O:27][CH:28]=[CH:29][N:30]=1>>[OH:8][N:9]([CH2:12][CH:13]([C:14]([N:21]1[CH2:25][CH2:24][CH2:23][CH:22]1[C:26]1[O:27][CH:28]=[CH:29][N:30]=1)=[O:16])[CH2:17][CH2:18][CH2:19][CH3:20])[CH:10]=[O:11]

Participants

3

Reactant 2

HCID 22256535HCID 22256535, compoundHCID 55299025HCID 55299025, compound

Product 1

HCID 22256527HCID 22256527, compound

Procedure

The title compound is prepared from 2-[(benzyloxy-formyl-amino)-methyl]-hexanoic acid D-7 (R=n-butyl) and 2-(S)-pyrrolidine-2-yl-oxazole E-5 (prepared as described in Procedure E) according to General Procedure D.

Workup

  1. custom(prepared as described in Procedure E)

Sources & evidence

ORD record
ord-0706c6ecba794ccca7f4a3ebf1627ed2
Source dataset
uspto-grants-2006_01
Patent number
US06987104B2

Reaction notes

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