HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085830Generated: October 27, 2026
N-BOC-ethylenediamine → t-Butyl [2-(2-amino-5-phenyl-4-thiazolecarboxamido)ethyl]carbamate
https://huagongshe.com/reaction/1085830
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | Methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate | HCID 664327 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | t-Butyl [2-(2-amino-5-phenyl-4-thiazolecarboxamido)ethyl]carbamate | HCID 54052891 | 45.1% |
Reaction Steps
5.0 g (21.3 mmol) of methyl 2-amino-5-phenyl-4-thiazolecarboxylate (which was prepared as described in J. Chem. Soc. Perk. Trans. I (1982) 159-164) and 6.84 g (42.7 mmol) of t-butyl (2-aminoethyl)carbamate were heated under reduced pressure for 2 hours at a bath temperature of 140°, whereby the methanol formed was distilled off continuously. After cooling the residue was dissolved in 50 ml of methylene chloride and chromatographed on 200 g of silica gel with a 9:1 mixture of methylene chloride and methanol as the eluting agent. The fractions which were pure according to the thin-layer chromatogram were combined and evaporated under reduced pressure, whereby there were obtained 4.5 g of a red, crystallizing oil. Crystallization from methanol and an ether/hexane mixture yielded 3.48 g (45%) of t-butyl [2-(2-amino-5-phenyl-4thiazolecarboxamido)ethyl]carbamate as beige crystals which were used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011849 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-3ff7e91cdcca4fb68e4c2864663acb2c |
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| Source note | uspto-grants-1991_04 |
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