HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433048Generated: October 25, 2026
Diisopropylethylamine → 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester
https://huagongshe.com/reaction/1433048
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzyl 1-methyl-2-oxoethylcarbamate | HCID 563116 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | methyl (2S)-2-aminopentanoate hydrochloride | HCID 14118488 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester | HCID 69027995 | 38.6% |
Reaction Steps
To a solution of [1-methyl-2-oxo-ethyl]-carbamic acid benzyl ester (12.3 g, 69 mmol) and norvaline methylester hydrochloride (11.6 g, 69 mmol) in MeOH (300 mL) is added diisopropyl ethyl amine (9.4 g, 73 mmol) and 2 drops of acetic acid. After 10 min., ZnCl2 (9.46 g, 69 mmol) and sodium cyanoborohydride (8.72 g, 14 mmol) is added. The solution is stirred at ambient for 16 h. The solution is then concentrated. The residue is dissolved in EtOAc and 1N KHSO4. The organic layer is washed with 1N KHSO4, H2O, and sat. NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatograghy eluting with a gradient of 20% EtOAc/hexane to 40% EtOAc/hexanes. The title compound (8.6 gm, 26.6 mmol) is obtained as a foam. MS (ion spray) m/z 323, (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612075B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-aa4a4c2600c048e99a1e0176bd434d07 |
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| Source note | uspto-grants-2009_11 |
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