HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272227Generated: October 30, 2026
Diethyl cyanophosphonate → HCID 178472025, compound
https://huagongshe.com/reaction/272227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoic acid hemihydrochloride dihydrate | HCID 131727188 | — |
| Reactant | HCID 178476472 | HCID 178476472 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178472025 | HCID 178472025 | 26% |
Reaction Steps
To a solution of 4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoic acid hemihydrochloride dihydrate (39.6 mg, 104.0 mmol) in DMF (1.2 mL) were added diethyl cyanophosphonate (20.6 μL, 136.1 μmol) and DIEA (36.0 μL, 209.4 μmol). The solution was stirred at ambient temperature for 3 hours, when (S)-2-[(2-aminoethyl)phenoxyphosphinoylamino]propionic acid ethyl ester mono acetic acid salt (mixture of diastereomers at phosphorus; 104.0 μmol) in DMF (200 μL) was added. The solution was stirred for 30 minutes when complete consumption of the starting materials was observed. An aliquot (66%) of the reaction was purified by silica gel chromatography using MeOH—CH2Cl2 (10-30%), yielding 27.2 mg of crude product. A small amount of the product (10 mg) was repurified by RP HPLC on C18 column using H2O/acetonitrile (2-95%) to provide 4.2 mg (26%) of the pure product. 1H NMR (300 MHz, DMSO-d6) δ 1.11 (t, 3H, J=6.9 Hz), 1.18 (d, 3H, J=7.2 Hz), 2.06-2.17 (m, 2H), 3.20 (s, 3H), 3.51 (m, 2H), 3.88 (m, 1H), 4.02 (m, 2H), 4.79 (s, 2H), 5.61 (m, 1H), 6.80 (d, 2H, J=9 Hz), 6.98 (br s, 1H), 7.18 (m, 3H), 7.32 (m, 2H), 7.67 (d, 2H, J=9 Hz), 8.20 (br s, 1H), 8.59 (s, 1H) 31P (121.4 MHz, DMSO-d6) δ 29.5, 30.1. MS (m/z) 608.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452901B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-8103cbd8993c4006aa52a74261be18e7 |
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| Source note | uspto-grants-2008_11 |
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