Cycloheptanone Oxime → HCID 59939376, compound

HRID 635281Notes

Reaction equation

HRID 635281 reaction equation
[C:1]1(=[N:8][OH:9])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:10]1([CH:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][C:29](OCC)=O)[CH2:22][CH2:21]2)[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1>>[C:10]1([CH:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][CH2:28][C:29]3[O:9][N:8]=[C:1]4[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][C:2]=34)[CH2:22][CH2:21]2)[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1

Participants

3

Reactant 2

HCID 137457Cycloheptanone OximeHCID 17773137HCID 17773137, compound

Product 1

HCID 59939376HCID 59939376, compound

Procedure

By the same reaction and treatment as in Example 48 using cycloheptanone oxime and ethyl 4-(4-(1-naphthyl)piperidin-1-yl)-n-butyrate, 3-(3-(4-(1-naphthyl)piperidin-1-yl)propyl-5,6,7,8-tetrahydro-4H-cyclohepta[c]isoxazole is obtained.

Sources & evidence

ORD record
ord-45059375d8a444f6bff15582c6b2ef58
Source dataset
uspto-grants-2001_02
Patent number
US06187774B1

Reaction notes

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