HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626655Generated: November 1, 2026
Methyl chloroformate → methyl 2-chloro-4-morpholino-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate
https://huagongshe.com/reaction/1626655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-chloro-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)morpholine trifluoroacetate | HCID 86663163 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 2-chloro-4-morpholino-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate | HCID 86663169 | — |
Reaction Steps
To a stirring solution of 4-(2-chloro-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)morpholine trifluoroacetate (intermediate 20) (2.16 g, 2.0 mmol) in DMF (10 ml), was added Et3N (560 uL, 4.0 mmol). Reaction mixture was stirred at room temperature (20° C.) for 2 minutes followed by the addition of methylchloroformate (186 uL, 2.4 mmol) followed by stirring at room temperature overnight. The reaction mixture was basified (with 2M NaOH) before partitioning between water (25 ml) and DCM (50 ml). The organic layer was recovered, passed through a hydrophobic frit and the solvent removed in vacuo, affording the title compound as a brown solid used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785457B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-43855ddbb17246edba0d1364d4cc62dd |
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| Source note | uspto-grants-2014_07 |
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