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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675829Generated: October 30, 2026

Triethylamine → HCID 86618945, compound

https://huagongshe.com/reaction/1675829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantN-Boc-4-chloro-D-phenylalanineHCID 7018791—
ReactantHCID 67339039HCID 67339039—
SolventDichloromethaneHCID 6344—
ProductHCID 86618945HCID 8661894588%

Reaction Steps

To a solution of (R)-5-methyl-4-((S)-2-methylpiperazin-1-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidine dihydrochloride (32 mg, 0.14 mmol) in DCM (5 mL) were added triethylamine (1 mL), (R)-2-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid (41 mg, 0.14 mmol) and HBTU (52 mg, 0.14 mmol). The mixture was stirred at room temperature for 1 hour. The solvent was removed and the residue was purified by silica gel chromatography, eluting with ethyl acetate to afford tert-butyl (R)-3-(4-chlorophenyl)-1-((S)-3-methyl-4-((R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)-1-oxopropan-2-ylcarbamate (60 mg, 88%). 1H NMR (CDCl3, 400 MHz) δ 8.44 (s, 1H), 7.23-7.01 (m, 4H), 5.40-5.15 (m, 1H), 4.85-4.60 (m, 1H), 4.46-4.30 (m, 1H), 4.20-4.00 (m, 1H), 3.82-3.60 (m, 1H), 3.40 (m, 1H), 3.00-2.70 (m, 2H), 2.28 (m, 1H), 1.70 (m, 1H), 1.40 (s, 9H), 1.30-0.98 (m, 6H). MS (APCI+) [M+H] +514.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003651B2
Source datasetuspto-grants-2011_08
ORD IDord-4dc1a7669ae449e8967f60a68be74db6
Source noteuspto-grants-2011_08