HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acid → HCID 9829495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acid | HCID 10847814 | — |
| Reactant | HCID 12151023 | HCID 12151023 | — |
| Product | HCID 9829495 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06303620B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-d5041a37c9e848b997bc670469e7b594 |
| Source note | uspto-grants-2001_10 |