HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525036Generated: October 25, 2026
Disodium 2,3-dihydroxybutanedioate → (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate
https://huagongshe.com/reaction/525036
Participants
| Role | Name | HCID | Charge |
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| Reactant | Disodium 2,3-dihydroxybutanedioate | HCID 13355 | — |
| Reactant | 4-Aminotetrahydropyran | HCID 419223 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate | HCID 86722033 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-tert-Butyl 1-oxo-1-(2-(tetrahydro-2H-pyran-4-yl carbamoyl)-1H-pyrrol-1-ylamino)propan-2-ylcarbamate | HCID 86722055 | — |
Reaction Steps
Tetrahydro-2H-pyran-4-amine (900 microl, 8.69 mmols) was added to a solution of (S)-methyl 1-(2-(tert-butoxycarbonylamino)propanamido)-1H-pyrrole-2-carboxylate (900 mg, 2.89 mmols, preparation 109) in toluene (36 ml). A 2M solution of Trimethyl aluminium in toluene (7 ml, 14.00 mmols) was added and it was stirred at 80° C. overnight. Water (50 ml) and a 0.5M solution of sodium tartrate (25 ml) were added. It was extracted with ethylacetate. The combined organic layers were washed with water and brine. It was dried, filtered and concentrated in vacuum. The title compound was obtained (617 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340547B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-04de8d8e819c4455b3734c36e5918338 |
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| Source note | uspto-grants-2016_05 |
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