HCID 18960878, compound → HCID 18960855, compound

HRID 1708120Notes

Reaction equation

HRID 1708120 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[Cl:7][C:8]1[CH2:13][CH2:12][NH:11][CH2:10][C:9]=1[C:14]1[CH:18]=[CH:17][O:16][N:15]=1.C(N1CCC(Cl)=C(C2C[CH:37]([O:39][CH2:40]C)ON=2)C1)(=O)C1C=CC=CC=1>>[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[Cl:7][C:8]1[CH2:13][CH2:12][NH:11][CH2:10][C:9]=1[C:14]1[CH:18]=[C:17]([CH2:37][O:39][CH3:40])[O:16][N:15]=1

Participants

3

Reactant 2

HCID 18960878HCID 18960878, compoundHCID 18960904HCID 18960904, compound

Product 1

HCID 18960855HCID 18960855, compound

Procedure

4-Chloro-3-(3-isoxazolyl)-1,2,5,6-tetrahydropyridine oxalate starting from 1-benzoyl-4-chloro-3-(5-ethoxy-4,5-dihydro-3-isoxazolyl)-1,2,5,6-tetrahydropyridine. M.p. 195°-196° C.

Sources & evidence

ORD record
ord-1222526442a24b44bb35ac6fe8f44e99
Source dataset
uspto-grants-1994_10
Patent number
US05356912

Reaction notes

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