1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidine → HCID 178476338, compound

HRID 2410379Notes

Reaction equation

HRID 2410379 reaction equation
[OH:1][C:2]1[C:7]2[C:8]([O:11][CH2:12][CH:13]3[CH2:18][CH2:17][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:15][CH2:14]3)=[N:9][O:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[C:26]([O:29][CH2:30][C@H:31]1[CH2:36][CH2:35][C@H:34](O)[CH2:33][CH2:32]1)(=[O:28])[CH3:27].OCCC1CCN(C(OC(C)(C)C)=O)CC1>>[C:26]([O:29][CH2:30][C@@H:31]1[CH2:36][CH2:35][C@H:34]([O:1][C:2]2[C:7]3[C:8]([O:11][CH2:12][CH:13]4[CH2:14][CH2:15][N:16]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:17][CH2:18]4)=[N:9][O:10][C:6]=3[CH:5]=[CH:4][CH:3]=2)[CH2:33][CH2:32]1)(=[O:28])[CH3:27]

Participants

4

Reactant 3

HCID 8541401-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 136263840HCID 136263840, compoundHCID 178476339HCID 178476339, compound

Product 1

HCID 178476338HCID 178476338, compound

Procedure

The title compound was prepared according to the procedure described in Step 2 of EXAMPLE 7 using tert-butyl 4-{[(4-hydroxy-1,2-benzisoxazol-3-yl)oxy]methyl}piperidine-1-carboxylate (EXAMPLE 17, step 2) and (trans-4-hydroxycyclohexyl)methyl acetate (EXAMPLE 46, Step 1) instead of 4-(benzyloxy)-1,2-benzisoxazol-3-ol and tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate.

Sources & evidence

ORD record
ord-3dfe16aa91424ce2afa33f0aba25913c
Source dataset
uspto-grants-2014_08
Patent number
US08816090B2

Reaction notes

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