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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953443Generated: November 4, 2026

1-(Morpholine-4-carboxamido)cyclohexanecarboxylic acid → N-[(S)-1-amino-1,2-dioxo-3-heptyl]-1-[N-[(2-methyl-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxamide

https://huagongshe.com/reaction/1953443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Morpholine-4-carboxamido)cyclohexanecarboxylic acidHCID 11507137—
ReactantHCID 21971170HCID 21971170—
Reactant(2RS, 3S)-3-amino-2-hydroxyheptanamideHCID 54092353—
Reactant1-[N-[4-(2-methy-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxylic acidHCID 131721985—
ProductN-[(S)-1-amino-1,2-dioxo-3-heptyl]-1-[N-[(2-methyl-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxamideHCID 1549090963%

Reaction Steps

The same reaction procedure as in Example 1 was repeated except that the 1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxylic acid used in Example 1 was replaced by 1.06 g of 1-[N-[4-(2-methy-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxylic acid, and (2RS,3S)-N-(2-methyl-2-propyl)-3-amino-2-hydroxyheptanamide used in Example 1 was replaced by 0.43 g of (2RS, 3S)-3-amino-2-hydroxyheptanamide synthesized in Reference Example 16, whereby 0.92 g of N-[(S)-1-amino-1,2-dioxo-3-heptyl]-1-[N-[(2-methyl-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxamide was obtained in a yield of 63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117870
Source datasetuspto-grants-2000_09
ORD IDord-a6043d5aff40404894d1df3de8704acd
Source noteuspto-grants-2000_09