HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243587Generated: October 30, 2026
N,N-Dimethylglycine → HCID 10412210, compound
https://huagongshe.com/reaction/1243587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 8-Chloro-1-(3,4,5,6-tetrahydro-2h-[1,2']bipyridinyl-4-yl)-5,6-dihydro4h-2,3,5,10b-tetraaza-benzo[e]azulene | HCID 11326488 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 10412210 | HCID 10412210 | 57.8% |
Reaction Steps
A solution of HBTU (152 mg, 0.38 mmol) in N,N-dimethylacetamide (1.9 ml) was added to a solution of the amine of example 4 (97 mg, 0.26 mmol), triethylamine (1.5 μl, cat.) and dimethylamino-acetic acid (36 mg, 0.26 mmol) in N,N-dimethylacetamide (2.5 ml) and heated to 50° C. for 2 hours. The mixture was cooled and the solvent evaporated under reduced pressure. The residue was partitioned between dichloromethane (10 ml) and 2M aqueous sodium hydroxide solution (10 ml). The organic phase was dried over magnesium sulphate before being evaporated under reduced pressure and purified by chromatography on silica gel using methanol and ammonium hydroxide in dichloromethane (7:1:93) as eluant to afford the title compound (70 mg) as a brown foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07119088B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-d2e7c397bd374516a3fae32572939a4c |
|---|
| Source note | uspto-grants-2006_10 |
|---|