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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808779Generated: October 30, 2026

Boc-L-Valine → HCID 67773033, compound

https://huagongshe.com/reaction/1808779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoc-L-ValineHCID 83693—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3,3-Difluoropyrrolidine hydrochlorideHCID 24903482—
SolventDimethylformamideHCID 6228—
ProductHCID 67773033HCID 6777303399.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-2-(Tert-butoxycarbonylamino)-3-methylbutanoic acid (1.1 g, 5.06 mmol), which is commercially available, and TBTU (1.63 g, 5.06 mmol) was mixed in DMF (10 mL). The mixture was cooled to 0° C. and TEA (2.105 mL, 15.19 mmol) was added. After 10 min was 3,3-difluoropyrrolidine hydrochloride (0.872 g, 6.08 mmol) added. The resultant mixture was stirred at rt over night. The mixture was concentrated and the residue dissolved in DCM (50 mL). The organic phase was washed with HCl (1M aq. solution, 100 mL), NaHCO3 (saturated, 2×100 mL) and brine (100 mL), filtered through a phase separator and concentrated under reduced pressure to give the title compound (1.54 g, 99%). The obtained crude product was used without further purification. 1H NMR (400 MHz, CD3OD) δ 0.77-1.09, 1.21, 1.43, 1.84-2.08, 2.22-2.69, 3.52-4.40. Total no of protons: 24. LCMS (M+H)+: 307.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361998B2
Source datasetuspto-grants-2013_01
ORD IDord-f07a9b76f88d4604a48d9c76966a59a1
Source noteuspto-grants-2013_01