HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470319Generated: November 1, 2026
1-Hydroxybenzotriazole → HCID 178520339, compound
https://huagongshe.com/reaction/1470319
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | n-Chloroaniline | HCID 258030 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 178525222 | HCID 178525222 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178520339 | HCID 178520339 | — |
Reaction Steps
To a solution of 2-(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidin-5-yl)acetic acid, 12-d, (150 mg, 0.68 mmol) and HOBt (101.2 mg, 0.75 mmol) in DMF (5 ml) was added EDC.HCl (144 mg, 0.75 mmol) and DIEPA (264 mg, 2.05 mmol). The solution was stirred at room temperature for 5 mins before the addition of the chlorophenyl amine (0.75 mmol) (Sigma-Aldrich). The mixture was stirred at room temperature for 24 hours. The mixture was then diluted with water and extracted with ethyl acetate. The organic layer was concentrated under vacuum and the residue was purified by silica gel column or Prep-HPLC to give the final compound 12-1. 1H NMR (DMSO-d6, 300 MHz): δ 10.23 (s, 1H), 8.56 (d, 1H), 7.92 (s, 1H), 7.63 (d, 2H), 7.37 (d, 2H), 6.64 (s, 1H), 3.53 (s, 2H). (M+H)+=330.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006433B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-e19de86f8470455a86201044e41b580d |
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| Source note | uspto-grants-2015_04 |
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