HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636673Generated: October 30, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 178502742, compound
https://huagongshe.com/reaction/636673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Ornithine, N2-[(1,1-dimethylethoxy)carbonyl]-N5-[imino[[(4-methylphenyl)sulfonyl]amino]methyl]- | HCID 83767 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178502742 | HCID 178502742 | 70% |
Reaction Steps
To a suspension of Boc-Arg(Tos)—OH (2 g, 4.7 mmol) in DMF (20 mL) at 0° C. is added MeNHOMe.HCl (1 g, 10.3 mmol), DIEA (6 mL) and BOP (2.5 g, 5.6 mmol). The solution is stirred at 0° C. for 10 h. DMF is evaporated by vacuum. The oily residue is dissolved in EtOAc (200 mL) and water (20 mL). The organic layer is washed with sat. NaHCO3, water (20 mL), 1 M HCl (10 mL) and sat. NaCl (2×20 mL). The organic layer is dried over MgSO4, filtered and evaporated to give a suspension. The suspension is filtered, washed with cold EtOAc (10 mL) and dried to give Boc-Arg(Tos)-N(Me)OMe (1.5 g, 70% yield). FAB-MS (M+H)+=472
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06194435B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-cf3eacdd6b2b431cae06c59714f05959 |
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| Source note | uspto-grants-2001_02 |
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