HCID 18629332, compound → HCID 86589543, compound

HRID 1635097Notes

Reaction equation

HRID 1635097 reaction equation
C([O:3][C:4]([C:6]1[C:15](=[O:16])[N:14]2[C:9]([C:10]([O:18][CH3:19])=[C:11](Cl)[CH:12]=[CH:13]2)=[C:8]([CH:20]2[CH2:22][CH2:21]2)[CH:7]=1)=[O:5])C.C([NH:30][CH2:31][CH2:32][CH:33]1[CH2:37][CH2:36][NH:35][CH2:34]1)(OC(C)(C)C)=O>>[NH2:30][CH2:31][CH2:32][CH:33]1[CH2:37][CH2:36][N:35]([C:11]2[CH:12]=[CH:13][N:14]3[C:9]([C:10]=2[O:18][CH3:19])=[C:8]([CH:20]2[CH2:21][CH2:22]2)[CH:7]=[C:6]([C:4]([OH:3])=[O:5])[C:15]3=[O:16])[CH2:34]1

Participants

3

Reactant 2

HCID 18629332HCID 18629332, compoundHCID 21955469tert-butyl N-[2-(pyrrolidin-3-yl)ethyl]carbamate

Product 1

HCID 86589543HCID 86589543, compound

Procedure

A series of procedures similar to Example 1 above is carried out, using Ethyl-8-chloro-1-cyclopropyl-9-methoxy-4-oxo-4H-quinolizine-3-carboxylate (Precursor B) and 3-(N-boc-aminoethyl)pyrrolidine (Precursor D) as the starting materials.

Sources & evidence

ORD record
ord-9f993c375e924b86a905a615e342518c
Source dataset
uspto-grants-2003_01
Patent number
US06509349B1

Reaction notes

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