HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86753660, compound → HCID 178496046, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86753660 | HCID 86753660 | — |
| Reactant | HCID 178496047 | HCID 178496047 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 178496046 | HCID 178496046 | 61.8% |
Reaction Steps
The intermediate tert-butyl N-(3-((2-methoxyacetimidoyl) aminomethyl)benzyl)carbamate (360 mg) prepared from tert-butyl N-(3-(aminomethyl)benzyl carbamate and intermediate G analogous to example 1 was deprotected in trifluoroacetic acid at 20° C. for 16 h. The crude product was purified by C18 reverse phase chromatography eluting with water (0.1% trifluoroacetic acid) to yield 150 mg of N-(3-(Aminomethyl)benzyl)-2-methoxyacetamidine as a yellowed, viscous oil (freeze-dried). Mass spectrum (CI) 208.0 (MH+, 100%). 1H NMR (200 MHz, D2O) δ 7.5-7.3 (m, 4H), 4.57 (s, 2H), 4.37 (s, 2H), 4.15 (s, 2H), 3.44 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE037438E1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-d355283def344428b46a6ffae78127c2 |
| Source note | uspto-grants-2001_11 |