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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249949Generated: October 29, 2026

Diisopropylethylamine → Arylaminoethyl amide deriv. 36

https://huagongshe.com/reaction/2249949

Reaction equation

Participants

RoleNameHCIDCharge
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—
Reactant3-Benzylsulfanyl-2-(R)-[(morpholine-4-carbonyl)-amino]-propionic acidHCID 54237934—
ReactantHCID 59733160HCID 59733160—
SolventDichloromethaneHCID 6344—
ProductArylaminoethyl amide deriv. 36HCID 114668456.4%

Reaction Steps

3-Benzylsulfanyl-2-(R)-[(morpholine-4-carbonyl)-amino]-propionic acid (182 mg, 0.56 mmol, 1.2 eq.), N1-(4-Trifluoromethoxy-phenyl)-(S)-propane-1,2-diamine from Scheme 1a (110 mg, 0.47 mmol, 1.0 eq.), and HATU (185 mg, 0.56 mmol, 1.2 eq.) were dissolved in CH2Cl2 (2 mL) at room temperature. DIPEA (245 μL, 1.41 mmol, 3.0 eq.) was added via syringe and the resulting mixture was monitored by LC/MS to completion. After the reaction was complete, the solvent was evaporated and directly purified by mass-directed HPLC and provided 22 mg (0.03 mmol, 5%) of a off-white solid (mono-TFA salt): HPLC-MS calcd. for C25H31F3N4O4S (M+H+) 541.2. found 541.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314872B2
Source datasetuspto-grants-2008_01
ORD IDord-a901d12b883b4a65ad54dd7a552ac9af
Source noteuspto-grants-2008_01