HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174921Generated: October 25, 2026
Diisopropylethylamine → 4'-Fluoro-biphenyl-4-carboxylic acid [2-(3-dimethylamino-pyrrolidin-1-yl)-benzooxazol-5-yl]-amide
https://huagongshe.com/reaction/1174921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(4-Fluorophenyl)benzoic acid | HCID 2782689 | — |
| 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 | 2-(3-Dimethylamino-pyrrolidin-1-yl)-benzooxazol-5-ylamine | HCID 68771730 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4'-Fluoro-biphenyl-4-carboxylic acid [2-(3-dimethylamino-pyrrolidin-1-yl)-benzooxazol-5-yl]-amide | HCID 76601343 | 77.2% |
Reaction Steps
Combine 2-(3-dimethylamino-pyrrolidin-1-yl)-benzooxazol-5-ylamine (0.100 g, 0.406 mmol), 4-(4-fluorophenyl)benzoic acid (0.073 g, 0.338 mmol), and HATU (0.129 g, 0.338 mmol) in CH2Cl2 and add DIEA (0.18 mL, 1.01 mmol). Shake the mixture in a shaker block at 40° C. for 72 h. Dilute the reaction mixture with CH2Cl2 (30 mL), and wash with saturated NaHCO3 (aqueous) (2×25 mL). Dry the organic phase over anhydrous sodium sulfate, filter, and concentrate in vacuo. Subject the crude product to flash column chromatography (40 g column) eluting with 8% MeOH/CH2Cl2, to yield the title compound as a bluish-white solid (0.116 g, 65%). mass spectrum (m/e): 445.3 [M+1], 443.3 [M−1]. 1H NMR (400 MHz, DMSO-d6): δ 10.23 (s, 1H), 8.05 (d, 2H, J=8.4 Hz), 7.85-7.79 (m, 4H), 7.75 (d, 1H, J=2.2 Hz), 7.41-7.30 (m, 4H), 3.79 (dd, 1H, J=9.9, 7.1 Hz), 3.72 (m, 1H), 3.54 (m, 1H), 3.31 (m, 1H), 2.86 (m, 1H), 2.25-2.12 (m, 7H), 1.86 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838543B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-6cd2e36e257c4dbc97ea84c360779d5b |
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| Source note | uspto-grants-2010_11 |
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