HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611804Generated: November 2, 2026
Benzyltrimethylammonium methoxide → HCID 178457138, compound
https://huagongshe.com/reaction/1611804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyltrimethylammonium methoxide | HCID 8504 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | (S)-2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide | HCID 15517727 | — |
| Reactant | HCID 178457506 | HCID 178457506 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178457138 | HCID 178457138 | 18.3% |
Reaction Steps
A solution of N-isopropylhistidine (302 mg, 1.53 mmol), (S)-2-amino-3-(4-benzyloxy-phenyl)-N-tert-butyl-propionamide (500 mg, 1.32 mmol), and benzyltrimethylammonium methoxide (40% solution in methanol, 2.1 mL, 3.36 mmol) in 10 mL dry DMF was cooled to 3° C. Then, HBTU (581 mg, 1.53 mmol) was added and the resulting mixture stirred at 3° C. for 60 minutes, warmed to 25° C., diluted with 35 mL diethyl ether, and washed with saturated aqueous sodium bicarbonate solution (35 mL) as well as with brine (35 mL), dried over anhydrous sodium sulfate, and concentrated at reduced pressure. The residue thus obtained was further purified twice by silica gel chromatography using 10% methanol in chloroform as eluant, to give 122 mg (13%) of the title compound as the dihydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06989448B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-4390baddfdb144a19b0baa3503e7163d |
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| Source note | uspto-grants-2006_01 |
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