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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360098Generated: October 30, 2026

N-[(pent-4-en-1-yloxy)carbonyl]-norleucine → N-[(but-3-en-1-yloxy)carbonyl]-L-norleucine

https://huagongshe.com/reaction/1360098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[(pent-4-en-1-yloxy)carbonyl]-norleucineHCID 45378373—
Reactant(2S)-2-{[(prop-2-en-1-yloxy)carbonyl]amino}hexanoic acidHCID 51340333—
ProductN-[(but-3-en-1-yloxy)carbonyl]-L-norleucineHCID 57617067—

Reaction Steps

The title compound was prepared in a manner similar to Example 1 (Steps 1-8). N-[(but-3-en-1-yloxy)carbonyl]-L-norleucine was prepared according to the procedure used for [(4-pentenyloxy)carbonyl]-L-norleucine (Example 3), and was used in place of N-[(allyloxy)carbonyl]-L-norleucine. 1H NMR (500 MHz, MeOH-d4) ppm: 8.58 (s, 1H), 8.42 (s, 1H), 8.09 (m, 3H), 7.96 (d, 1H), 7.74 (m, 4H), 6.70 (d, J=15.2 Hz, 1H), 6.39 (m, 1H), 5.87 (m, 2H), 5.29 (d, 1H), 5.10 (d, 1H), 4.80 (m, 2H), 4.71 (m, 2H), 4.57 (t, 1H), 4.07 (m, 2H), 2.86 (dd, 1H), 2.70 (m, 1H), 2.55 (m, 1H), 2.48 (t, 1H), 2.17 (dd, 1H), 1.85 (m, 1H), 1.79-1.64 (m, 2H), 1.55-1.37 (m, 5H), 1.01 (t, 3H). LRMS (CI, [M+H]) Calc'd=653.4. found=653.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879797B2
Source datasetuspto-grants-2011_02
ORD IDord-6ffd468abbb547b1b0eb40ca8793b638
Source noteuspto-grants-2011_02