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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239556Generated: October 30, 2026

PyBOP → HCID 69350912, compound

https://huagongshe.com/reaction/2239556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyBOPHCID 2724699—
Reactant2-(1-(Tert-butoxycarbonyl)azetidin-3-yl)acetic acidHCID 11095989—
SolventDimethylformamideHCID 6228—
ProductHCID 69350912HCID 6935091257.5%

Reaction Steps

PyBOP (1.946 g, 3.74 mmol) was added to a solution of [1-(tert-Butoxycarbonyl)azetidin-3-yl]acetic acid (0.805 g, 3.74 mmol) in DMF (10 mL). The mixture was stirred in an ice-bath, ammonia gas was bubbled in for 3 mins and then the mixture was stirred at rt overnight. The reaction mixture was concentrated, water (15 mL) and saturated, aqueous NaHCO3 (5 mL) were added, and the mixture was extracted with EtOAc (20 mLx3). The extracts were combined, washed with water (20 mL) and brine (10mL), dried (Na2SO4) and evaporated. Column chromatography of the residue (ISOLUTE SI, 50 g/150 ml), eluting with EtOAc and heptane (50:50), then EtOAc and then MeOH and EtOAc (1:99, 2:98 and 5:95), gave the title compound (0.461 g, 57.5%) as a white solid. 1H NMR (400 MHz, CDCl3): 1.42 (s, 9H), 2.53 (d, 2H), 2.85-2.96 (m, 1H), 3.60 (dd, 2H), 4.09 (t, 2H), 5.78 (s, br, 2H); 13C NMR (100 MHz, CDCl3): 25.4, 28.3, 39.7, 54.3 (br), 79.4, 156.3, 173.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723333B2
Source datasetuspto-grants-2010_05
ORD IDord-2a35efec385e489fb61b9702a909444d
Source noteuspto-grants-2010_05