HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxypropylamine → HCID 16493899, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxypropylamine | HCID 1672 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-Boc-L-Leucine Hydrate | HCID 12373896 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 16493899 | HCID 16493899 | 92% |
Reaction Steps
Isobutyl chloroformate (520 μL, 4.0 mmol) was added to a solution of N-Boc leucine monohydrate (1.0 g, 4.0 mmol) and N-methyl morpholine (440 μL, 1.73 mmol) in THF at 0° C. After two minutes, 3-methoxypropylamine (410 μL, 4.0 mmol) was added and the mixture was allowed to warm to rt. After thirty minutes, the reaction mixture was filtered through a bed of celite and all volatiles were removed under reduced pressure to yield N-Boc-L-leucine-3-methoxypropyl amide (1.10 g, 92%) as a white solid. 1H NMR: (CDCl3) δ 0.93, 6H, d; 1.42, 9H, s; 3.35, 3H, s; 3.38, 2H, d; 3.43 m 2H, t; 4.03m 1H, m; 4.39, s, 1H; 4.91, 1H, m; 6.60, 1H, m,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07037916B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-88ca1f7ec8cf4b0f88bcc26f11e1e80d |
| Source note | uspto-grants-2006_05 |