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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282902Generated: October 30, 2026

Diisopropylethylamine → HCID 118696282, compound

https://huagongshe.com/reaction/2282902

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—
ReactantHCID 52271561HCID 52271561—
ReactantN-[(3R,4S,5S)-3-methoxy-1-{(2S)-2-[(1R,2R)-1-methoxy-2-methyl-3-oxo-3-{[(1S)-2-phenyl-1-(1,3-thiazol-2-yl)ethyl]amino}propyl]pyrrolidin-1-yl}-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamideHCID 86685731—
SolventDichloromethaneHCID 6344—
ProductHCID 118696282HCID 11869628237.9%

Reaction Steps

According to the general procedure D, from #86 (300 mg, 0.45 mmol, 1 eq.), #169 (106 mg, 0.45 mmol, 1 eq.), dichloromethane (10 mL), HATU (194 mg, 0.54 mmol, 1.2 eq.) and diisopropylethylamine (117 mg, 0.9 mmol, 2 eq.) was synthesized the crude desired material, which was purified by reverse phase chromatography (Method P) to afford #193 (149 mg, 37%) as a white solid. HPLC (Protocol X): m/z 873.4 [M+H+], retention time=3.34 minutes (purity=98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138486B2
Source datasetuspto-grants-2015_09
ORD IDord-c2195a6d138343ef9d8925e98e9b28af
Source noteuspto-grants-2015_09