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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256808Generated: October 30, 2026

L-Glutamine → Boc-L-Valine

https://huagongshe.com/reaction/2256808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-GlutamineHCID 5961—
ReactantL-ThreonineHCID 6288—
ReactantL-TryptophanHCID 6305—
ReactantL-IsoleucineHCID 6306—
Reactant1,2-EthanedithiolHCID 10902—
ReactantL-ProlineHCID 145742—
ProductBoc-L-ValineHCID 83693—

Reaction Steps

A larger excess of 6 to 8 equivalents is used in the coupling of steps (h) and (m) with the tert-butoxycarbonyl-protected amino acids aparagine, glutamine, isoleucine, proline, and threonine. In the cycles following addition of a tryptophane residue, 2% 1,2-ethanedithiol (FLUKA) is added to the deprotection steps (a) and (b) in order to prevent the oxidation of the indole ring. Dehydration of the carboxamide function of glutamine is minimized by preforming the 1-hydroxybenzotriazole ester (0°, 15 min) before addition to the resin in step (h).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656596
Source datasetuspto-grants-1997_08
ORD IDord-c03513d166bf4d9d933f5a2eda0b8657
Source noteuspto-grants-1997_08