HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67353085, compound → tert-Butyl [(1R,3S)-3-aminocyclopentyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67353085 | HCID 67353085 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonia | HCID 222 | 0% |
| Product | tert-Butyl [(1R,3S)-3-aminocyclopentyl]carbamate | HCID 45091934 | 56% |
Reaction Steps
Following the procedure for ((1R,3R)-3-amino-cyclopentyl)-carbamic acid tert-butyl ester the title compound was prepared from ((1R,3S)-3-allyloxycarbonylamino-cyclopentyl)-carbamic acid tert-butyl ester with further purification by column chromatography on silica gel (gradient: 0 to 5% methanol in DCM then 0 to 10% 2M NH3 in methanol solution in DCM) to afford 300 mg (56%) of ((1R,3S)-3-amino-cyclopentyl)-carbamic acid tert-butyl ester. LCMS (Method I, ESI): RT=0.32 min, m+H-Boc=101.2; 1H NMR (400 MHz, DMSO) δ: 6.84 (s, 1H), 3.77-3.69 (m, 1H), 3.21 (m, 2H), 2.00 (m, 1H), 1.78-1.63 (m, 2H), 1.50 (m, 1H), 1.37 (s, 9H), 1.17 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461328B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-2c80160adc8b4582bb48d055449e6883 |
| Source note | uspto-grants-2013_06 |