Cyclopentylacetyl chloride → HCID 57954405, compound

HRID 221360

Reaction equation

HRID 221360 reaction equation
N1CCC(O[CH2:8][C:9]2[O:13][N:12]=[C:11]([C:14]3[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=3)[N:10]=2)CC1.[CH:20]1([CH2:25][C:26](Cl)=[O:27])[CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH:20]1([CH2:25][C:26]([N:10]2[CH2:11][CH2:14][CH:8]([C:9]3[O:13][N:12]=[C:11]([C:14]4[CH:15]=[CH:16][N:17]=[CH:18][CH:19]=4)[N:10]=3)[CH2:8][CH2:9]2)=[O:27])[CH2:24][CH2:23][CH2:22][CH2:21]1

Participants

3

Reactant 2

HCID 3485182Cyclopentylacetyl chlorideHCID 579543974-[5-(Piperidin-4-yloxymethyl)-[1,2,4]oxadiazol-3-yl]-pyridine

Product 1

HCID 57954405HCID 57954405, compound

Procedure

4-[5-(Piperidin-4-yloxymethyl)-[1,2,4]oxadiazol-3-yl]pyridine (Example 51) was reacted with cyclopentylacetyl chloride, in a similar manner to that described in Example 55, to afford the title compound: RT=3.44 min, m/z (ES+)=341.3 [M+H]+.

Sources & evidence

ORD record
ord-a616ccc788074adca47bb0f078ad85bb
Source dataset
uspto-grants-2012_06
Patent number
US08207147B2

Linked notes

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