HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364792Generated: October 30, 2026
Diisopropylcarbodiimide → (S)-2,5-dioxopyrrolidin-1-yl 2-(methoxycarbonylamino)-3-methylbutanoate
https://huagongshe.com/reaction/2364792
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid | HCID 10942966 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-2,5-dioxopyrrolidin-1-yl 2-(methoxycarbonylamino)-3-methylbutanoate | HCID 86649102 | 77% |
Reaction Steps
To a mixture of (S)-2-(methoxycarbonylamino)-3-methylbutanoic acid (19.66 g, 112 mmol) and N-hydroxysuccinimide (13.29 g, 116 mmol) was added ethyl acetate (250 ml), and the mixture was cooled to 0-5° C. Diisopropylcarbodiimide (13.88 g, 110 mmol) was added and the reaction mixture was stirred at 0-5° C. for about 1 hour. The reaction mixture was warmed to room temperature. The solids (diisopropylurea by-product) were filtered and rinsed with ethyl acetate. The filtrate was concentrated in vacuo to an oil. Isopropyl alcohol (200 ml) was added to the oil and the mixture was heated to about 50° C. to obtain a homogeneous solution. Upon cooling, crystalline solids formed. The solids were filtered and washed with isopropyl alcohol (3×20 ml) and dried to give the title compound as a white solid (23.2 g, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691938B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-79d792d05cd04d878dae94a9ae495b2e |
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| Source note | uspto-grants-2014_04 |
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