HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631826Generated: October 30, 2026
N-BOC-ethylenediamine → Ethyl 2-[2-(tert-butoxycarbonylamino)ethylamino]-5-methylamino-thiazole-4-carboxylate
https://huagongshe.com/reaction/631826
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | 3'-O-ethyl-N,N-diisopropylphosphoramidite | HCID 195451 | — |
| Reactant | Ethyl 2-bromo-5-(methylamino)-1,3-thiazole-4-carboxylate | HCID 53613688 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-[2-(tert-butoxycarbonylamino)ethylamino]-5-methylamino-thiazole-4-carboxylate | HCID 89825793 | — |
Reaction Steps
Ethyl 2-bromo-5-methylamino-thiazole-4-carboxylate (546 mg, 2.059 mmol) and tert-butyl N-(2-aminoethyl)carbamate (1.3 g, 8.11 mmol) were combined in anhydrous 1,4-dioxane (15 ml). EDIPA (3 ml, 17.2 mmol) was added and the mixture was heated in a sealed tube for 23 hours at 100° C. The mixture was cooled to room temperature and partitioned between DCM and a saturated solution of sodium bicarbonate. Layers were separated, the aqueous phase was extracted twice with DCM and the combined organic layers were dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica, gradient of 30 to 100% ethyl acetate in heptane) to yield 185 mg (0.537 mmol, 26%) MS(ESI) m/z=345.2 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321724B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-6c7966313d6e483986bb44f2c77ff9be |
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| Source note | uspto-grants-2016_04 |
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