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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077584Generated: November 1, 2026

N,N-Dimethylglycine → HCID 57584921, compound

https://huagongshe.com/reaction/2077584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 57584985HCID 57584985—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57584921HCID 5758492133.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-(6-chloro-5-(dimethylamino)pyridin-3-yl)benzo[d]thiazol-2-amine (70 mg, 230 μmol), HATU (210 mg, 552 μmol), and 2-(dimethylamino)acetic acid (45 mg, 436 μmol) in DMF (2.5 mL) was heated to 60° C. for 2 h. The solution was diluted with H2O (20 mL) until it became cloudy and cooled to rt. The mixture was filtered, washed with H2O (10 mL), Na2HCO3 (saturated, 5 mL), and H2O (5 mL). The filter was dissolved in MeOH (10%) in DCM and dried over MgSO4. The organic was filtered, concentrated to a yellow solid. This was further purified on silica using MeOH in EtOAc (0-5%) to give a light yellow solid. A second purification with 1:1 hexane-acetone removed the less polar impurity (NAc) effectively, affording a white solid (30 mg). MS (ESI, POS. ION) M/Z: calc'd for C18H20ClN5OS: 389.1. found: 390.1. 1H NMR (400 MHz, chloroform-d) δ ppm 2.43 (s, 3H) 2.93 (s, 3H) 3.25 (s, 2H) 7.52 (d, J=2.15 Hz, 1H) 7.63 (dd, J=8.41, 1.76 Hz, 1H) 7.87 (d, J=8.41 Hz, 1H) 7.99 (d, J=1.56 Hz, 1H) 8.27 (d, J=2.15 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928140B2
Source datasetuspto-grants-2011_04
ORD IDord-d14c0c53cfe943cba27aac85516c4cac
Source noteuspto-grants-2011_04