Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911850Generated: November 3, 2026

2-Pyridineethanamine → HCID 86670467, compound

https://huagongshe.com/reaction/1911850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridineethanamineHCID 75919—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 67971935HCID 67971935—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86670467HCID 86670467—

Reaction Steps

2-(2-Aminoethyl)pyridine (0.034 mL, 0.29 mmol) was added to a stirred, room temperature mixture of 4-({(2S,5R)-1-(tert-butoxycarbonyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidin-2-yl}methyl)benzoic acid (100 mg, 0.190 mmol), HATU (87 mg, 0.228 mmol), and DIPEA (0.166 mL, 0.951 mmol) in DMF (1.9 ml). The resulting mixture was stirred at room temperature overnight. Upon completion, as determined by LC-MS, water was added, and the mixture was partitioned with EtOAc. The aqueous layer was extracted with EtOAc (3×), and the combined organic layers were washed with brine, dried with Na2SO4, filtered, and concentrated in vacuo to give the product that was used directly in the next step. LC-MS=630.3 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604038B2
Source datasetuspto-grants-2013_12
ORD IDord-700f5e266e644f879d8d4dd7327ded6c
Source noteuspto-grants-2013_12