HCID 86662525, compound → HCID 66763157, compound

HRID 573751Notes

Reaction equation

HRID 573751 reaction equation
[Si:1]([O:8][C@H:9]1[CH2:18][C:17]([CH3:20])([CH3:19])[CH2:16][C:15]2[N:14]=[C:13]([CH:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)[C:12]([CH:26]=[O:27])=[C:11]([I:28])[C:10]1=2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:29]([C:33]1[CH:34]=[C:35]([Mg]Br)[CH:36]=[CH:37][CH:38]=1)([CH3:32])([CH3:31])[CH3:30]>>[Si:1]([O:8][C@H:9]1[CH2:18][C:17]([CH3:20])([CH3:19])[CH2:16][C:15]2[N:14]=[C:13]([CH:21]3[CH2:22][CH2:23][CH2:24][CH2:25]3)[C:12]([CH:26]([C:37]3[CH:36]=[CH:35][CH:34]=[C:33]([C:29]([CH3:32])([CH3:31])[CH3:30])[CH:38]=3)[OH:27])=[C:11]([I:28])[C:10]1=2)([C:4]([CH3:5])([CH3:6])[CH3:7])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 86662525HCID 86662525, compoundHCID 178440903HCID 178440903, compound

Product 1

HCID 66763157HCID 66763157, compound

Procedure

Obtained by starting from (S)-5-(tert-butyldimethylsilyloxy)-2-cyclopentyl-4-iodo-7,7-dimethyl-5,6,7,8-tetrahydroquinoline-3-carbaldehyde and 3-tert.-butylphenylmagnesium bromide. The product is obtained as a diastereomic mixture, which is used directly in the next step.

Workup

  1. customObtained
  2. customThe product is obtained as a diastereomic mixture, which

Sources & evidence

ORD record
ord-f3ba127c13724db0a094a1f28685aa0b
Source dataset
uspto-grants-2015_05
Patent number
US09029544B2

Reaction notes

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