HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870599Generated: October 29, 2026
Triethylamine → 3-Chloropropyl 2-(indan-2-ylamino)-5,7-dihydropyrrolo[3,4-d]pyrimidine-6-carboxylate
https://huagongshe.com/reaction/870599
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carbonochloridic acid, 3-chloropropyl ester | HCID 69399 | — |
| Reactant | N-(2,3-dihydro-1H-inden-2-yl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-amine dihydrochloride hydrate | HCID 86726534 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloropropyl 2-(indan-2-ylamino)-5,7-dihydropyrrolo[3,4-d]pyrimidine-6-carboxylate | HCID 86726562 | 100.5% |
Reaction Steps
Add a solution of 3-chloropropyl carbonochloridate (0.55 mL; 1.48 equiv; 4.54 mmoles) in tetrahydrofuran (21 mL) dropwise over 1 hour to a mixture of N-(2,3-dihydro-1H-inden-2-yl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-amine dihydrochloride hydrate (1.0 g; 1.0 equiv; 3.07 mmoles) and triethylamine (2.2 mL; 5.1 equiv; 15.78 mmoles) in tetrahydrofuran (21 mL). Stir the solution for 18 hours, then dilute with dichloromethane and wash with sodium bicarbonate solution. Further extract the aqueous layer with dichloromethane (2×). Dry the combined organic extracts over sodium sulfate, filter, and concentrate to afford 3-chloropropyl 2-(indan-2-ylamino)-5,7-dihydropyrrolo[3,4-d]pyrimidine-6-carboxylate (1.15 g; 100%) as a brown solid: MS (m/z): 373(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969555B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-8abc660695a14709aa402b66588318c5 |
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| Source note | uspto-grants-2015_03 |
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