HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(N-Boc)-(2-aminoethyl)azetidine → benzyl N-[3-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]azetidine-1-carboximidoyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(N-Boc)-(2-aminoethyl)azetidine | HCID 37818431 | — |
| Reactant | benzyl N-[3-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]azetidine-1-carboximidoyl]carbamate | HCID 140379072 | — |
| Product | benzyl N-[3-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethyl]azetidine-1-carboximidoyl]carbamate | HCID 140387135 | — |
Reaction Steps
The title compound was prepared from 3-(N-tert-butyloxycarbonylaminoethyl) azetidine according the procedure for 3-(N-tert-butyloxycarbonylaminomethyl)-1-(N-benzyloxycarbon ylamidino) azetidine, in a yield of 0.090 g (34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723444 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-8f3a40523b2f4c598bcdee0f2ca4642e |
| Source note | uspto-grants-1998_03 |