HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108902Generated: October 29, 2026
(6-Nitro-benzothiazol-2-yl)-carbamic acid tert-butyl ester → HCID 58305681, compound
https://huagongshe.com/reaction/2108902
Participants
| Role | Name | HCID | Charge |
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| Reactant | (6-Nitro-benzothiazol-2-yl)-carbamic acid tert-butyl ester | HCID 58305710 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58305681 | HCID 58305681 | 77.2% |
Reaction Steps
6-Nitrobenzothiazol-2-yl tert-butyl carbamate (4.68 g, 15.8 mmol) was dissolved in dimethylformamide (120 mL) and palladium on charcoal (841 mg, 10% Pd, 0.79 mmol Pd) was added. The air was replaced with hydrogen (1 bar) and the mixture was vigorously stirred at 60° C. until completion of the reaction (2 h). The palladium was removed by filtration through a pad of celite and the solution was concentrated to 20 mL. Water (200 mL) was added. After stirring for 1 h, the precipitated 6-aminobenzothiazol-2-yl tert-butyl carbamate was filtered off and washed with water. Additional product was obtained by repeated filtration of the mother liquor. A total of 3.24 g (12.2 mmol, 77%) of a grey solid was obtained. LC/ESI-MS: m/z=266 [M+H]+; m/z=264 [M−H]−; Rt=2.54 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514460B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-a062798eb91d47fa9bc4e1a335b686dd |
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| Source note | uspto-grants-2009_04 |
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