HCID 25175821, compound → HCID 25175967, compound

HRID 2407293Notes

Reaction equation

HRID 2407293 reaction equation
O1C2C=CC=CC=2OCC1CN1CCCC(CO)(C)C1.[O:21]1[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[O:24][CH2:23][CH:22]1[CH2:31][N:32]1[CH2:37][CH2:36][CH2:35][C:34]([CH2:40][O:41][CH2:42][CH2:43][OH:44])([CH2:38]C)[CH2:33]1>>[O:21]1[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[O:24][CH2:23][CH:22]1[CH2:31][N:32]1[CH2:37][CH2:36][CH2:35][C:34]([CH2:40][O:41][CH2:42][CH2:43][OH:44])([CH3:38])[CH2:33]1

Participants

3

Procedure

Prepared from [1-(2,3-dihydrobenzo[1,4]dioxin-2-ylmethyl)-3-methylpiperidin-3-yl]methanol using the procedure described above for 2-[1-(2,3-dihydrobenzo[1,4]dioxin-2-ylmethyl)-3-ethylpiperidin-3-yl-methoxy]ethanol.

Sources & evidence

ORD record
ord-2f49a212fe17481ea5678b00c487e851
Source dataset
uspto-grants-2014_08
Patent number
US08809536B2

Reaction notes

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