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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380659Generated: November 1, 2026

(2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acid → HCID 9829495, compound

https://huagongshe.com/reaction/380659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acidHCID 10847814—
ReactantHCID 12151023HCID 12151023—
ProductHCID 9829495HCID 9829495—

Reaction Steps

4-Benzyl-1-((2R)-2-methylamino-3-(2-naphthyl)propionyl)piperidine-4-carboxylic acid methylamide (360 mg; 0.82 mmole) was coupled to (2E)-5-(tert-butyloxycarbonylamino)-5-methyl-2-hexenoic acid using the same coupling procedure as in step D. Removal of the N-terminal Boc group was performed as in step D but at −10° C. The crude product was purified on a RP-18-Seppak® (5 g; Waters) using a gradient from 0.1% TFA in water/acetonitrile 100/0 to 0.1% TFA in 60/40 water/acetonitrile to afford 306 mg of the title compound as a trifluoroacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303620B1
Source datasetuspto-grants-2001_10
ORD IDord-d5041a37c9e848b997bc670469e7b594
Source noteuspto-grants-2001_10