HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254106Generated: October 31, 2026
N-(tert-butoxycarbonyl)glycine → Glycyl-3-cyclohexyl-D-alanine
https://huagongshe.com/reaction/254106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2R)-2-amino-3-cyclohexylpropanoic acid | HCID 736026 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Glycyl-3-cyclohexyl-D-alanine | HCID 66842930 | 20.4% |
Reaction Steps
N-(tert-butoxycarbonyl)glycine (2.0 g, 11.4 mmol) and DIPEA (4.0 g, 31 mmol) were dissolved in methylene chloride (25 ml). TBTU (4.1 g, 12.8 mmol) was added and the mixture was stirred for 15 min at room temperature. 3-cyclohexyl-D-alanine (2.1 g, 12.2 mmol) was added and the reaction mixture was stirred over night at room temperature. The reaction mixture was transferred to a separation funnel and was then extracted with a water/acetic acid solution (100 ml 5% acetic acid). The organic layer was separated and evaporated under reduced pressure. The residue was dissolved in formic acid (20 ml) and the mixture was stirred over night at 40° C. The formic acid was removed under reduced pressure. The residue was washed with water (50 ml) and then stirred in aceton (25 ml) for 1 h at room temperature. The solid material was filtered off and washed with aceton (20 ml). 530 mg (20%) of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07871998B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-99a4504cc38f4f3187f4cea100a387ad |
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| Source note | uspto-grants-2011_01 |
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