Cyclobutylamine → HCID 16748073, compound

HRID 2084475Notes

Reaction equation

HRID 2084475 reaction equation
[CH:1]1([CH2:7][CH2:8][CH2:9][C@@H:10]([C:19]2[O:23][N:22]=[C:21]([CH2:24]OS(C3C=CC(C)=CC=3)(=O)=O)[N:20]=2)[CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:36]1([NH2:40])[CH2:39][CH2:38][CH2:37]1>>[CH:36]1([NH:40][CH2:24][C:21]2[N:20]=[C:19]([C@H:10]([CH2:9][CH2:8][CH2:7][CH:1]3[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]3)[CH2:11][C:12]([O:14][C:15]([CH3:17])([CH3:18])[CH3:16])=[O:13])[O:23][N:22]=2)[CH2:39][CH2:38][CH2:37]1

Participants

3

Reactant 2

HCID 75645CyclobutylamineHCID 16747945tert-Butyl (3R)-6-cyclohexyl-3-[3-({[(4-methylphenyl)sulfonyl]oxy}methyl)1,2,4-oxadiazol-5-yl]hexanoate

Product 1

HCID 16748073HCID 16748073, compound

Procedure

Method as for preparation 5 using tert-butyl (3R)-6-cyclohexyl-3-[3-({[(4-methylphenyl)sulfonyl]oxy}methyl)-1,2,4-oxadiazol-5-yl]hexanoate (preparation 177) (500 mg, 0.99 mmol) and cyclobutylamine (250 μl, 2.96 mmol) as starting materials.

Sources & evidence

ORD record
ord-424f5008987f4ec48cd67581dbf28ccf
Source dataset
uspto-grants-2004_04
Patent number
US06716861B2

Reaction notes

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