HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541812Generated: November 1, 2026
HCID 57961674, compound → tert-Butyl (3-{[(3-aminobenzoyl)amino]methyl}phenyl)carbamate
https://huagongshe.com/reaction/541812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57961674 | HCID 57961674 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | tert-Butyl (3-{[(3-aminobenzoyl)amino]methyl}phenyl)carbamate | HCID 57962529 | 130.5% |
Reaction Steps
To a solution tert-butyl (3-[{(3-nitrobenzoyl)amino]methyl}phenyl)carbamate (1.50 g, 4.04 mmol) in water (2.91 mL), methanol (16 mL) and acetic acid (6.2 mL) was added iron (0.564 g, 10.1 mmol) powder in small quantities. When the addition was completed, the mixture was stirred in water bath for 4 h, and the reaction was complete. The mixture was filtered, and the cake was washed with MeOH/EtOAc. The brown filtrate was concentrated and diluted with H2O, and the aqueous layer was extracted with EtOAc three times. The combined organic layers were dried, filtered and concentrated to give the desired product as a brown solid (1.8 g). LCMS for C19H23N3O3 (M+H)+: m/z=342.1. 1H NMR (400 MHz, CD3OD): δ 7.38 (t, J=2.0 Hz, 1H), 7.28 (ddd, J=8.0, 2.0, 1.2 Hz, 1H), 7.22 (t, J=8.0 Hz, 1H), 7.16 (s, 1H), 7.14 (t, J=8.0 Hz, 1H), 7.08 (m, 1H), 6.96 (ddd, J=8.0, 2.4, 1.2 Hz, 1H), 6.85 (ddd, J=8.0, 2.0, 1.2, 1H), 4.50 (s, 2H), 1.50 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871753B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-838975b104ee448ba61011c7c12ee6fb |
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| Source note | uspto-grants-2014_10 |
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