Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716408Generated: October 30, 2026

(S)-tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoate → (S)-tert-butyl 2-amino-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoate

https://huagongshe.com/reaction/716408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoateHCID 86689670—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(S)-tert-butyl 2-amino-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoateHCID 8668967283%

Reaction Steps

To a stirred solution of (S)-tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoate INT-8 (591 mg, 0.95 mmol) in EA (25 ml) was added Pd/C (101 mg, 0.09 mmol) and the suspension degassed with H2. The mixture was stirred vigorously under an atmosphere of H2 overnight then filtered through celite and the filtrate was concentrated to give 405 mg (83%) of (S)-tert-butyl 2-amino-3-(4-(5-(4-(heptyloxy)phenyl)pyrimidin-2-yl)phenyl)propanoate INT-9. LCMS-ESI (m/z) calculated for C30H39N3O3: 489.3. found: 490.2 [M+H]+, tR=2.35 min (Method 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187522B2
Source datasetuspto-grants-2015_11
ORD IDord-ced48cd657a24f24a545bbcbc0a70bd3
Source noteuspto-grants-2015_11