HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651084Generated: November 1, 2026
Ammonia → Ethanol, 2-[(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methoxy]-
https://huagongshe.com/reaction/1651084
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 3010393 | HCID 3010393 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethanol, 2-[(4-amino-5-iodo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methoxy]- | HCID 456429 | — |
Reaction Steps
4-Chloro-5-iodo-7-(2-hydroxyethoxymethyl)pyrrolo[2,3-d] pyrimidine (9b, 0.3 g) was covered with methanol saturated with ammonia (25 mL) and the reaction mixture was heated at 130 degrees C. in a sealed vessel for 10 hours. The solvent was concentrated in vacuo to give a semi-solid mass which was recrystallized from methanol to afford 12, 0.20 g (71.4%), mp 169-170 degrees C. 1H NMR (DMSO-d6): δ 8.7 (s, 1, C2-H), 8.3 (s, 1, C6-H), 5.7 (s, 2, N7-CH2) 4.6 (t, 1, J=4H3, exchangeable with D2O, OH): UVλmax nm(ε×104); (pH 7) 210 (2.0), 280 (0.9); (pH 1) 230 (1.8), 279 (0.9); (pH 11) 228 (0.9), 278 (0.9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927830 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-3962c8295b354560b6337dea97ecd143 |
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| Source note | uspto-grants-1990_05 |
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