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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254059Generated: October 30, 2026

4-Methylmorpholine → HCID 66842603, compound

https://huagongshe.com/reaction/254059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methyl-D-leucineHCID 6950508—
ReactantN-{[4-((2R,3R)-1-(4-Fluorophenyl)-3-{[2-(4-fluorophenyl)-2-oxoethyl]thio)-4-oxoazetidin-2-yl)phenoxy]acetyl}glycineHCID 66842760—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66842603HCID 6684260370.6%

Reaction Steps

N-{[4-((2R,3R)-1-(4-Fluorophenyl)-3-{[2-(4-fluorophenyl)-2-oxoethyl]thio}-4-oxoazetidin-2-yl)phenoxy]acetyl}glycine (20 mg, 0.037 mmol) was dissolved in 1.5 ml DMF. N-Methylmorpholine (13 μl, 118 mmol) and TBTU (15 mg, 0.047 mmol) were added and the mixture was stirred for 1 h., β-tert-Butyl-D-alanine (11 mg, 0.076 mmol) was added and the mixture was stirred for 3 h. Water (0.2 ml) was added and the mixture was stirred for 15 min. MeOH (2 ml) and NaBH4 (15 mg) were added. NH4Ac (ca 20 mg) was added after 15 min. Purification was performed using preparative HPLC on a C8 column. A gradient from 20-50% MeCN in 0.1M NH4Ac was used as mobile phase. Lyophilization yielded 17.5 mg (70%) of the title compound. M/z: 668 (M−1). NMR (400 MHz, DMSO): 8.24 (t, 1H), 7.77-7.87 (m, 1H), 7.32-7.40 (m, 4H), 7.22-7.27 (m, 2H), 7.07-7.19 (m, 4H), 6.99 (d, 2H), 5.06 (dd, 1H), 4.70-4.78 (m, 1H), 4.53 (s, 2H), 4.31 (dd, 1H), 4.09-4.17 (m, 1H), 3.65-3.81 (m, 2H), 2.84-3.00 (m, 2H), 1.65 (dd, 1H), 1.42 (dd, 1H), 0.86 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07871998B2
Source datasetuspto-grants-2011_01
ORD IDord-73fc40a8b7394838b283ee3229a7dbd1
Source noteuspto-grants-2011_01