HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47764Generated: October 28, 2026
Sodium borohydride → N-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]acetamide
https://huagongshe.com/reaction/47764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl (2RS)-2-acetylamino-3-(2-pyrazinyl)propanoate | HCID 86584440 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]acetamide | HCID 22747907 | 157.3% |
Reaction Steps
2.8 g of sodium borohydride are added to a solution of 8.5 g of ethyl (2RS)-2-acetylamino-3-(2-pyrazinyl)propanoate in 100 cm3 of ethanol and the mixture is then stirred at a temperature in the region of 20° C. After 18 hours, the reaction medium is taken up in 50 cm3 of water and 100 cm3 of dichloromethane and the aqueous phase is concentrated under reduced pressure (1 kPa) at a temperature in the region of 40° C. 11 g of N-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)-ethyl]acetamide are obtained in the form of a brown paste [1H NMR spectrum (300 MHz, (CD3)2SO-d6 with addition of a few drops of CD3COOD-d4 δ in ppm): 1.71 (s: 3H); 2.81 (dd, J=14.5 and 9 Hz: 1H); 3.03 (dd, J=14.5 and 5 Hz: 1H); 3.35 (dd, J=11 and 6 Hz); 3.42 (dd, J=11 and 5 Hz: 1H); 4.11 (mt: 1H); 7.75 (residual d, J=8.5 Hz: 0.5H); 8.45 (d, J=2.5 Hz: 1H); 8.50 (broad s: 1H); 8.53 (mt: 1H)]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699895B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-6b145cc4f362407e8cf44431c7156d5a |
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| Source note | uspto-grants-2004_03 |
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