HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355057Generated: November 1, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl 2-(3-hydroxypyrrolidin-1-yl)-1,3-thiazole-5-carboxylate
https://huagongshe.com/reaction/2355057
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-Hydroxypyrrolidine | HCID 98210 | — |
| Reactant | Methyl 2-bromothiazole-5-carboxylate | HCID 2773502 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-(3-hydroxypyrrolidin-1-yl)-1,3-thiazole-5-carboxylate | HCID 68452743 | — |
Reaction Steps
A mixture of methyl 2-bromo-1,3-thiazole-5-carboxylate (3 g, 13.5 mmol), 3-pyrrolidinol (1.3 g, 14.9 mmol) and DBU (4.1 mL, 27 mmol) in dioxane (50 mL) was heated at 80-85° C. overnight. After cooling, the mixture was diluted with water and extracted five times with EtOAc. The combined EtOAc extracts were washed with water, dried (Na2SO4) and concentrated to give the crude title compound as a light brown solid. 1H NMR (400 MHz, acetone-d6): δ 7.83 (s, 1H), 4.65 (m, 1 H), 4.33 (m, 1 H), 3.79 (s, 3 H), 3.67-3.45 (m, 4 H), 2.29-2.19 (m, 1 H), 2.11 (m, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754745B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-0ee2fea293eb49d7b3ceb6271daa3fbc |
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| Source note | uspto-grants-2010_07 |
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