HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157451Generated: October 27, 2026
1,2-Dichloroethane → HCID 59511757, compound
https://huagongshe.com/reaction/1157451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 2-Amino-N-isopropylacetamide | HCID 533849 | — |
| Reactant | HCID 68524390 | HCID 68524390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59511757 | HCID 59511757 | — |
Reaction Steps
A mixture of 2-amino-5-[(S)-(+)-3-hydroxy-2-methylpropoxy]benzoic acid hydrochloride (200 mg, 0.76 mmol), 2-amino-N-isopropylacetamide*HCl (INTERMEDIATE I.1) (105 mg, 0.70 mmol) and triethylamine (0.23 mL, 1.68 mmol) in DMF (5 mL) was stirred at room temperature for 5 min. EDC (176 mg, 0.92 mmol) and HOBt (124 mg, 0.92 mmol) were added and stirring continued at room temperature for 16 h. The mixture was partitioned between ethyl acetate and sat. NaHCO3 (aq.) and the aqueous extracted with additional ethyl acetate. The combined organics were washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The crude 2-amino-5-[(S)-(+)-3-hydroxy-2-methylpropoxy]-N-(isopropylcarbamoylmethyl)benzamide (INTERMEDIATE VIII.1) was used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807686B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-349a2737e5714664a84460541d331871 |
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| Source note | uspto-grants-2010_10 |
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