Ethyl chloroformate → HCID 19808500, compound

HRID 1885153Notes

Reaction equation

HRID 1885153 reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][NH2:21])[CH2:15][CH2:14]2)=[CH:5][CH:4]=1.[Cl:22][C:23]([O:25][CH2:26][CH3:27])=[O:24]>C(Cl)(Cl)Cl>[ClH:22].[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[N:13]2[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][NH:21][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:15][CH2:14]2)=[CH:5][CH:4]=1

Participants

4

Reactant 2

HCID 10928Ethyl chloroformateHCID 19808484HCID 19808484, compound

Product 1

HCID 19808500HCID 19808500, compound

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

This compound was prepared as indicated in the preceding example, from 1-(7-methoxy-1-naphthyl)-4-(2-aminoethyl)piperazine and ethyl chloroformate in chloroform.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-1e8b58ba02934eaca9713dd621cca5b1
Source dataset
uspto-grants-1992_09
Patent number
US05143916

Reaction notes

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