HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057337Generated: October 26, 2026
4-Methylmorpholine → HCID 178464214, compound
https://huagongshe.com/reaction/2057337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 178486031 | HCID 178486031 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178464214 | HCID 178464214 | 89.3% |
Reaction Steps
To 1 g (3.19 mmol) trans-5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexyl]-pentanoic acid in 37 ml CH2Cl2 was added 0.5 ml (4.8 mmol, 1.5 eq) diethylamine and 0.53 ml (4.79 mmol, 1.5 eq) NMM. The solution was cooled to 0° C. and 795 mg (4.15 mmol, 1.3 eq) EDCI and 98 mg (6.4 mmol) HOBT were added. The mixture was stirred at RT over night, partitioned between CH2Cl2 and a saturated aqueous solution of NaHCO3. The organic phase was washed with KHSO4 and brine, dried over Na2SO4 and evaporated. Column chromatography with EtOAc/hexane 1:1 gave 1.05 g (86%) trans-[4-(4-Diethylcarbamoyl-butyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester as colorless liquid MS: 369 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07335687B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-231401b3208947f4822f66320c416967 |
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| Source note | uspto-grants-2008_02 |
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