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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093113Generated: October 28, 2026

Dimethylamine → HCID 57904772, compound

https://huagongshe.com/reaction/1093113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTetrahydrofuranHCID 8028—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 57905300HCID 57905300—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 57904772HCID 57904772100%

Reaction Steps

To a solution of 5-benzyloxy-1-carboxymethoxy-6-oxo-3,7-diazatricyclo[7.2.2.02,7]trideca-2,4-diene-4-carboxylic acid ethyl ester (25 mg, 0.057 mmol) in DMF (1 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU) (43 mg, 0.11 mmol) and 4-(dimethylamino)pyridine (DMAP) (14 mg, 0.11 mmol) and the mixture stirred at room temperature for 15 min under N2. To this was added a 2M THF solution of dimethylamine (0.057 mL, 0.11 mmol) and the mixture stirred at room temperature for 90 min. The mixture was concentrated and the residue taken up in ethyl acetate (10 mL), washed with 1N HCl followed by brine, then dried (Na2SO4) and concentrated to provide the title compound (36 mg, 0.057 mmol, 100% yield) as a crude amber film: HPLC: retention time=2.15 min; LCMS: m/z 470 (M+H); 1H NMR (400 MHz, CDCl3) δ ppm 1.23 (3H, t, J=6.6 Hz), 1.65-1.76 (2H, m), 1.88-2.01 (2H, m), 2.11-2.26 (4H, m), 2.46 (1H, brs), 2.90 (3H, s), 2.95 (3H, s), 4.10 (2H, t, J=7.0 Hz), 4.23-4.33 (4H, m), 5.24 (2H, s), 7.27-7.38 (3H, m), 7.46 (2H, d, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129398B2
Source datasetuspto-grants-2012_03
ORD IDord-7c7938bab8d0475fa0d287e1eef247dc
Source noteuspto-grants-2012_03