HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748269Generated: October 31, 2026
Sodium hydride → diethyl 1-{4-[(tert-butoxycarbonyl)amino]butan-2-yl}-1H-indole-2,6-dicarboxylate
https://huagongshe.com/reaction/1748269
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diethyl 1H-indole-2,6-dicarboxylate | HCID 44754779 | — |
| Reactant | Tert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxide | HCID 86682388 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | diethyl 1-{4-[(tert-butoxycarbonyl)amino]butan-2-yl}-1H-indole-2,6-dicarboxylate | HCID 67236468 | 133.6% |
Reaction Steps
To a stirred suspension of 60% NaH dispersion in mineral oil (78.8 mg, 2.0 mmol) in DMF (2.5 mL) cooled to 0° C. is added a solution of diethyl 1H-indole-2,6-dicarboxylate (Intermediate A, 561 mg, 2.1 mmol) in DMF (3 mL). The mixture is stirred for 20 min and a solution of tert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxide (450 mg, 1.8 mmol) in DMF (2.5 mL) is added. The reaction mixture is stirred for 30 min at 0° C. and it is warmed to room temperature and stirred for 48 h. Saturated NH4Cl solution is added and the reaction mixture is extracted with EtOAc. The organic layer is separated, washed with water, then brine, dried (MgSO4) and concentrated to afford the title compound (1.04 g, 50% pure) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150577B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8c12f7bfa7754c81b77bf51e26af72f3 |
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| Source note | uspto-grants-2015_10 |
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