HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625794Generated: October 25, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-Amino-4-chlorobenzamide
https://huagongshe.com/reaction/625794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 2-Amino-4-chlorobenzoic acid | HCID 66646 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-4-chlorobenzamide | HCID 12374837 | 66.1% |
Reaction Steps
To solution of 2-amino-4-chlorobenzoic acid (4.4 g, 25.8 mmol) in degassed DMF (75 mL) were added successively HOBt (4.19 g, 31 mmol), DIEA (5.4 mL, 31 mmol), EDCI (5.37 g, 28 mmol), and 2N NH3/MeOH (18 mL, 36 mmol), and the solution was stirred at rt for 4 d. The mixture was concentrated under reduced pressure and the residue was partitioned between H2O (200 mL) and DCM (200 mL). The separated aqueous phase was extracted with DCM (2×200 mL) and the combined organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 10-50% EtOAc/hexanes to afford 2-amino-4-chlorobenzamide as a solid (2.91 g, 66%). 1H NMR (300 MHz, DMSO-d6) δ 6.50 (dd, J=8.48, 2.26 Hz, 1H), 6.75 (d, J=2.26 Hz, 1H), 6.84 (br s, 2H), 7.18 (br s, 1H), 7.48-7.63 (m, 1H), 7.80 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09308207B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d72b1f75fd1f44d6b1f9fef8d4d3dc64 |
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| Source note | uspto-grants-2016_04 |
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