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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225248Generated: November 1, 2026

Benzyloxycarbonylglycine → HCID 69287319, compound

https://huagongshe.com/reaction/2225248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonylglycineHCID 14349—
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 69285537HCID 69285537—
SolventAcetonitrileHCID 6342—
ProductHCID 69287319HCID 69287319—

Reaction Steps

A solution of crude dihydrobromide salt of (1R,3R,4S)-N1-isopropyl-3-(methoxymethyl)-N1-methylcyclohexane-1,4-diamine prepared according to the procedure of Example 4b, Step 2 (423 mg) in acetonitrile (5 mL) was treated with 2-(benzyloxycarbonylamino)acetic acid (259 mg), diisopropylethylamine (0.80 ml) and HATU (516 mg). The mixture was stirred overnight at rt, then was concentrated under vacuum. The residue was purified by reverse phase HPLC followed by lyopholization to provide benzyl 2-((1S,2R,4R)-4-(isopropyl(methyl)amino)-2-(methoxymethyl)cyclohexylamino)-2-oxoethylcarbamate (192 mg) as a white powder. MS found: (M+H)+=406.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378409B2
Source datasetuspto-grants-2008_05
ORD IDord-356170b7806e4a7e836a69c6cea3a839
Source noteuspto-grants-2008_05