HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227225Generated: October 26, 2026
Dimethylamine, hydrochloride → L-trans4Hydroxyproline N,N-dimethylamide hydrochloride
https://huagongshe.com/reaction/227225
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid | HCID 88804 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | L-trans4Hydroxyproline N,N-dimethylamide hydrochloride | HCID 131725849 | — |
Reaction Steps
To a solution of BOC-hydroxyproline (2.99 g, 13.89 mmol) in dichloromethane (100 ml) were added N,N-diisopropylethylamine (3.7 ml, 21.24 mmol), 4-(dimethylamino)pyridine (1.74 g, 14.24 mmol), dimethylamine hydrochloride (1.72 g, 21.09 mmol) and WSCDI (3.17 g, 16.68 mmol). The mixture was stirred at room temperature for 30 hr. The mixture was diluted with dichloromethane (100 ml) and washed with 0.3M KHSO4, saturated sodium bicarbonate solution and brine, dried over MgSO4, and concentrated in vacuo to give a colourless gum. This crude material was taken up in 4N HCl/dioxan (50 ml) and stirred at room temperature for 1 hr and then concentrated in vacuo. The residue was azeotroped with toluene and diethyl ether to give a white solid; yield 0.45 g (17%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560454B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-da9920f0bdc9413dba4c294c5971ecc5 |
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| Source note | uspto-grants-2009_07 |
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