HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029033Generated: October 31, 2026
Diisopropylethylamine → HCID 53329716, compound
https://huagongshe.com/reaction/1029033
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3R)-3-fluoropyrrolidine hydrochloride | HCID 2759162 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 71253315 | HCID 71253315 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53329716 | HCID 53329716 | — |
Reaction Steps
A solution of 2-(2-amino-3-morpholinoquinolin-6-yl)-3-(3,3-dimethylbutyl)benzoic acid hydrochloride (168 mg, 0.357 mmol) and HATU (204 mg, 0.536 mmol) in DMF (5 mL) was stirred for 10 min at RT. (R)-(−)-3-fluoropyrrolidine hydrochloride (224 mg, 1.787 mmol) and 1,1′-dimethyltriethylamine (0.622 mL, 3.57 mmol) were added and the reaction mixture was allowed to stir overnight at RT. The reaction mixture was partitioned between water and ethyl acetate. The organic phase was separated, dried over MgSO4 and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC (10-100% water with 0.1% TFA/CH3CN, 11 min). The obtained product was eluted on an SCX cartridge with MeOH followed by 2M NH3/MeOH. The basic fraction was concentrated to afford the titled compound as a white solid. MS (ESI, pos. ion) m/z: 505 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-f3f04fec83ec44d48fea81d6d1593184 |
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| Source note | uspto-grants-2014_05 |
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