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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953915Generated: November 3, 2026

Dimethylformamide → 3-(4-Benzyloxy-phenyl)-2-[4-methyl-2-(tetrahydro-pyran-4-ylamino)-pentanoylamino]-propionic acid tert-butyl ester

https://huagongshe.com/reaction/1953915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
ReactantFmoc-leucineHCID 1549133—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactanttert-butyl (2S)-2-amino-3-[4-(benzyloxy)phenyl]propanoateHCID 11151579—
SolventDiethyl EtherHCID 3283—
Product3-(4-Benzyloxy-phenyl)-2-[4-methyl-2-(tetrahydro-pyran-4-ylamino)-pentanoylamino]-propionic acid tert-butyl esterHCID 7006963170%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of FMOC-leucine (10.3 g, 29 mmol) in 300 mL of DMF was cooled to 0° C. and treated with diisopropylethyl amine (73 mL) and HBTU (11.1 g, 29.2 mmol). The resulting solution was stirred at 0° C. for 30 minutes and treated with (S)-2-amino-3-(4-benzyloxy-phenyl)-propionic acid tert-butyl ester (110 g, 36.9 mmol). The resulting solution was stirred for 30 minutes at 0° C. and warmed to room temperature. The reaction mixture was poured into 500 mL of ether and washed sequentially with IN aqueous HCl, saturated aqueous NaHCO3 (100 mL) and brine (5×100 mL). The organic phase was collected, dried over MgSO4 and concentrated to near dryness. The residue was triturated with hexane. The product was collected by suction filtration and air dried to give the title compound as a white solid (12.16 g, 70%); mp 158-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117841
Source datasetuspto-grants-2000_09
ORD IDord-73c711c945d94a228cae6bc8765913d2
Source noteuspto-grants-2000_09