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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360099Generated: October 31, 2026

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

https://huagongshe.com/reaction/1360099

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 1-7) and Example 2. N-[(But-3-en-1-yloxy)carbonyl]-L-norleucine was prepared according to the procedure used for [(4-pentenyloxy)carbonyl]-L-norleucine, and was used in place of N-[(allyloxy)carbonyl]-L-norleucine. 1H NMR (500 MHz, MeOH-d4) ppm: 8.59 (s, 1H), 8.34 (s, 1H), 8.10 (m, 3H), 7.96 (d, 1H), 7.77 (m, 4H), 5.82 (m, 2H), 5.30 (d, 1H), 5.10 (d, 1H), 4.82 (m, 2H), 4.64 (m, 2H), 4.59 (t, 1H), 4.10 (m, 2H), 3.80 (m, 1H), 3.08 (m, 1H), 2.88 (m, 2H), 2.60 (m, 1H), 2.19 (dd, 1H), 1.90-1.63 (m, 6H), 1.50-1.40 (m, 5H), 0.95 (t, 3H). LRMS (CI, [M+H]) Calc'd=655.4. found=655.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879797B2
Source datasetuspto-grants-2011_02
ORD IDord-f7d766a657ad4c4c862e1d3705b3ea8b
Source noteuspto-grants-2011_02