HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Morpholine-4-carboxamido)cyclohexanecarboxylic acid | HCID 11507137 | — |
| Reactant | HCID 21971170 | HCID 21971170 | — |
| Reactant | (2RS, 3S)-3-amino-2-hydroxyheptanamide | HCID 54092353 | — |
| Reactant | 1-[N-[4-(2-methy-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxylic acid | HCID 131721985 | — |
| Product | N-[(S)-1-amino-1,2-dioxo-3-heptyl]-1-[N-[(2-methyl-2-propyloxycarbonyl)piperadine-4-carbonyl]amino]cyclohexanecarboxamide | HCID 15490909 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117870 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-a6043d5aff40404894d1df3de8704acd |
| Source note | uspto-grants-2000_09 |