HCID 20436877, compound → HCID 131712183, compound

HRID 444057Notes

Reaction equation

HRID 444057 reaction equation
[Cl:1][CH2:2]/[CH:3]=[CH:4]/[CH2:5][CH2:6][C:7]([NH:9][CH:10]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[O:8].NC(CCCCSCC(OCC)=O)C(OCC)=O>>[Cl:1][CH2:2]/[CH:3]=[CH:4]\[CH2:5][CH2:6][C:7]([NH:9][CH:10]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])=[O:8]

Participants

3

Reactant 2

HCID 20436877HCID 20436877, compoundHCID 20436953HCID 20436953, compound

Product 1

HCID 131712183HCID 131712183, compound

Procedure

Diethyl 4-chlorobut-2E-enylacetamidomalonate (Chem. Eng. Data. (1970) (205), respectively, in an analogous manner to that described above for diethyl 2-amino-7-thia-nonanedioate, and used in Examples 64 to 66.

Sources & evidence

ORD record
ord-3e28667ab06946a59b939911e8748104
Source dataset
uspto-grants-1981_04
Patent number
US04262128

Reaction notes

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