HCID 68579996, compound → HCID 68579945, compound

HRID 2233869Notes

Reaction equation

HRID 2233869 reaction equation
[NH2:1][C:2]([C:4]1[S:8][C:7]([N:9]2[CH2:14][CH2:13][CH:12]([NH:15]C(=O)OC(C)(C)C)[CH2:11][CH2:10]2)=[N:6][CH:5]=1)=[O:3].Cl.[Cl:24]C1C(Cl)=C(C)NC=1C(NC1CCNCC1)=O>>[ClH:24].[NH2:15][CH:12]1[CH2:13][CH2:14][N:9]([C:7]2[S:8][C:4]([C:2]([NH2:1])=[O:3])=[CH:5][N:6]=2)[CH2:10][CH2:11]1

Participants

3

Reactant 2

HCID 68579996HCID 68579996, compoundHCID 68582510HCID 68582510, compound2×

Product 1

HCID 68579945HCID 68579945, compound

Procedure

Title compound was synthesized from tert-butyl 1-[5-(aminocarbonyl)-1,3-thiazol-2-yl]piperidin-4-ylcarbamate (Intermediate 82) by an analogous method to Intermediate 1.

Sources & evidence

ORD record
ord-efc0d2e191b9443895d8bde0502a2e1a
Source dataset
uspto-grants-2010_05
Patent number
US07709503B2

Reaction notes

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