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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270989Generated: October 31, 2026

1-Pyrrolidineethanamine → HCID 58843188, compound

https://huagongshe.com/reaction/1270989

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanamineHCID 1344—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantBoc-L-beta-homovalineHCID 2761559—
ReactantHCID 69432149HCID 69432149—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58843188HCID 5884318878%

Reaction Steps

{(R)-2-Methyl-1-[(2-pyrrolidin-1-yl-ethylcarbamoyl)-methyl]-propyl}-carbamic acid tert-butyl ester. HOBT (0.351 g, 2.6 mmol) and EDCl (0.5 g, 2.6 mmol) were added to a solution of (R)-3-tert-butoxycarbonylamino-4-methyl-pentanoic acid (0.4 g, 1.7 mmol) in DMF (8.5 mL). Following the addition of a solution of 2-pyrrolidin-1-yl-ethylamine (0.3 g, 2.6 mmol) in DMF (2 mL), N-methyl-morpholine (0.26 g, 2.6 mmol) was added dropwise. The reaction mixture was stirred at rt overnight. Water (20 mL) and EtOAc (30 mL) were then added to the mixture. The aqueous layer was extracted with EtOAc (3×40 mL). The combined organic layers were washed with 1 N NaOH (2×20 mL) and brine (40 mL), dried (MgSO4), and concentrated. Purification by column chromatography [0–20% (1% NH4OH/MeOH)/CH2Cl2] afforded 0.44 g (78%) of the desired product. MS (electrospray): mass calculated for C17H33N3O3, 327.25; m/z found, 328.3 [M+H]+. 1H NMR (400 MHz, CDCl3): 6.22 (s, 1H), 5.30 (d, J=6.7 Hz, 1H), 3.66–3.59 (m, 1H), 3.44–3.36 (m, 1H), 3.35–3.27 (m, 1H), 2.59–2.56 (m, 2H), 2.52 (m, 4H), 2.42–2.40 (m, 2H), 1.87–1.74 (m, 8H), 1.43 (s, 9H), 0.93 (t, J=6.3, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202269B2
Source datasetuspto-grants-2007_04
ORD IDord-9fe270316542468e978cdd5c681d24af
Source noteuspto-grants-2007_04