HCID 22256526, compound → HCID 86587586, compound

HRID 1431950Notes

Reaction equation

HRID 1431950 reaction equation
CC1(C)[O:6][C:5](=[O:7])[CH:4]([CH:8]([CH2:12][CH2:13][CH2:14][CH3:15])[C:9]([OH:11])=O)[O:3]1.[NH:17]1[CH2:21][CH2:20][CH2:19][C@H:18]1[C:22]1[O:23][CH:24]=[CH:25][N:26]=1>>[OH:3][C@@H:4]([C@H:8]([C:9]([N:17]1[CH2:21][CH2:20][CH2:19][C@H:18]1[C:22]1[O:23][CH:24]=[CH:25][N:26]=1)=[O:11])[CH2:12][CH2:13][CH2:14][CH3:15])[C:5]([OH:6])=[O:7]

Participants

3

Reactant 2

HCID 22256526HCID 22256526, compoundHCID 55299025HCID 55299025, compound

Product 1

HCID 86587586HCID 86587586, compound

Procedure

The title compound is prepared from 2-(2,2-dimethyl-4-oxo-1,3-dioxolan-5-yl)hexanoic acid B-5 and 2-(S)-pyrrolidin-2-yl-oxazole A-5 (synthesis is described in Procedure E) according to General Procedure B.

Workup

  1. custom(synthesis is described in Procedure E)

Sources & evidence

ORD record
ord-7f72424fcd7746e7bff83143375ca9e6
Source dataset
uspto-grants-2009_11
Patent number
US07612059B2

Reaction notes

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