HCID 89824859, compound → HCID 89825121, compound

HRID 62233Notes

Reaction equation

HRID 62233 reaction equation
[CH3:1][N:2]([CH3:36])[CH:3]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH:25]1C[CH:26]1[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH2:4][O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12].CN(C)C(COCCCCCCCC)COCCCCCCCCC1CC1CCCCCCC(OC)=O>>[CH3:36][N:2]([CH3:1])[CH:3]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]/[CH:25]=[CH:26]\[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH2:4][O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12]

Participants

3

Procedure

Ketone (q) may also be carried forward to methyl 6-(2-(dimethylamino)-3-((8-(2-octylcyclopropyl)octyl)oxy)propoxy)hexanoate (Compound 22) in a manner analogous to that described above for Compound 2.

Sources & evidence

ORD record
ord-6735be7d0d0d4993a7b56cdfde3d5a63
Source dataset
uspto-grants-2016_09
Patent number
US09446132B2

Reaction notes

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