HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498837Generated: November 4, 2026
Sodium hydride → Methyl 1-amino-3-chloro-1h-pyrrole-2-carboxylate
https://huagongshe.com/reaction/1498837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-chloro-1H-pyrrole-2-carboxylate | HCID 5324605 | — |
| Reactant | O-(Diphenylphosphinyl)hydroxylamine | HCID 10955453 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-amino-3-chloro-1h-pyrrole-2-carboxylate | HCID 22179993 | 91.5% |
Reaction Steps
To a suspension of sodium hydride (60 percent, 1.5 g, 37.5 mmol) in DMF (250 mL) was added methyl 3-chloro-1H-pyrrole-2-carboxylate (5.0 g, 31.3 mmol) at 0° C., and the mixture was stirred for 25 min, followed by the addition of O-(diphenylphosphoryl)hydroxylamine (10.0 g, 43.75 mmol). The reaction mixture was stirred at RT for 4 h and quenched by aq. Na2SO3 solution. After stirred for another 5 min, the mixture was extracted with EtOAc (3×300 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to give crude product as a brown oil, which was purified by chromatography purification on silica gel (PE:EA=4:1) to obtain the title compound (5.00 g, 91%) as a white solid. MS (ES+) C6H7ClN2O2 requires: 174, 176. found: 175, 177 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200002B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-381a8a5d8a2548ecae4fa94a30e81e31 |
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| Source note | uspto-grants-2015_12 |
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