HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415239Generated: October 28, 2026
Hydrochloric Acid → HCID 86633089, compound
https://huagongshe.com/reaction/415239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86633090 | HCID 86633090 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86633089 | HCID 86633089 | 3% |
Reaction Steps
To a solution of methyl 2-(4-methoxyphenylbenzo[d]oxazole-7-carboxylate in DMF (15 mL) was added HOBt (148 mg, 1.1 mmol), NH4Cl (54 mg, 1.0 mmol), DIPEA (387 mg, 3.0 mmol) and EDCI (211 mg, 1.1 mmol). The mixture was stirred at 25° C. for 10 hr. To the resulting mixture, water (10 mL) and aqueous hydrochloric acid (1 N) were added to pH=3, then extracted with ethyl acetate (100 mL×4). The organic phase was washed with saturated sodium bicarbonate solution and brine, concentrated, and dried in vacuum. The crude product was purified by pre-HPLC to obtain 2-(4-methoxyphenylbenzo[d]oxazole-7-carboxamide as a white solid (8 mg, yield 3% for 2 steps). 1H-NMR (400 MHz, CDCl3-d) δ 3.93 (s, 3H), 6.16 (s, 1H), 7.06-7.08 (d, J=8 Hz, 3H), 7.47 (s, 1H), 7.90-8.18 (m, 4H); LC-MS (ESI) m/z 269 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088760B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c828d6b7b0d049cf82e5ab5c52215922 |
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| Source note | uspto-grants-2012_01 |
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