Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480554Generated: October 30, 2026

Diisopropylethylamine → HCID 66845588, compound

https://huagongshe.com/reaction/1480554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant(S)-2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-2-(4-chlorophenyl)acetic acidHCID 59564918—
Reactant(5R,7R)-5-methyl-4-(piperazin-1-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-ol dihydrochlorideHCID 66618034—
SolventDichloromethaneHCID 6344—
ProductHCID 66845588HCID 6684558889%

Reaction Steps

(S)-2-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-2-(4-chlorophenyl)acetic acid (0.1765 g, 0.5194 mmol) was combined with (5R,7R)-5-methyl-4-(piperazin-1-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-7-ol dihydrochloride (0.1596 g, 0.5194 mmol) and then slurried in methylene chloride (4.5 mL). The suspension was treated with diisopropylethylamine (0.2714 mL, 1.558 mmol) then with HBTU (0.1970 g, 0.5194 mmol), and the mixture was stirred at ambient temperature for 16 hours. The reaction was quenched with 10% Na2CO3 and then separated. The aqueous portion was washed twice with dichloromethane. The combined organic portions were dried with Na2SO4 and concentrated in vacuo. The residue was subjected to chromatography on SiO2 eluting with 4% MeOH/dichloromethane to yield (S)-tert-butyl 2-((S)-1-(4-chlorophenyl)-2-(4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)-2-oxoethyl)pyrrolidine-1-carboxylate (0.256 g, 89%). MS (ESI+) [M+H] 556.1/558.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409886B2
Source datasetuspto-grants-2016_08
ORD IDord-335c6ffbc8a64a449e0dc8760054fb58
Source noteuspto-grants-2016_08