HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671565Generated: October 27, 2026
N,N-Dimethylglycine → 2-Dimethylamino-N-[2-((R)-indan-1-ylamino)-quinolin-5-yl]-acetamide
https://huagongshe.com/reaction/1671565
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | (R)-N2-Indan-1-yl-quinoline-2,5-diamine | HCID 44219082 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Dimethylamino-N-[2-((R)-indan-1-ylamino)-quinolin-5-yl]-acetamide | HCID 44219397 | 58.3% |
Reaction Steps
To a stirred solution of N,N-dimethylglycine (124 mg, 1.2 mmol) in dichloromethane (20 ml) and DMF (10 ml) were added at room temperature N-ethyldiisopropylamine (452 mg, 3.5 mmol) and TBTU (514 mg, 1.6 mmol) and the mixture was allowed to stir for 90 min. (R)—N2-indan-1-yl-quinoline-2,5-diamine (example 16) (275 mg, 1.0 mmol) was added and the reaction mixture was allowed to stir for 17 h, poured into sat. NaHCO3 solution (30 ml) and extracted with dichloromethane (2×30 ml). The combined organic layers were washed with water (30 ml), dried (MgSO4) and evaporated. The crude product was further purified by flash chromatography on silica gel (heptane/ethyl acetate) and crystallization (ethyl acetate/heptane) to yield the title compound as white solid (210 mg, 58%). M.p. 153° C.; MS: m/e=361.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994324B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4914b469b81f45018743d5e59e6502c5 |
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| Source note | uspto-grants-2011_08 |
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