HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087063Generated: October 31, 2026
Hydrochloric Acid → HCID 178446380, compound
https://huagongshe.com/reaction/2087063
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pentanal | HCID 8063 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 16-({[5-(aminomethyl)-4-hydroxy-3-methoxytetrahydro-2-furanyl]oxy}{5-[2,4-dioxo-3,4-dihydro-1 (2H)-pyrimidinyl]-3,4-dihydroxytetrahydro-2-furanyl}methyl)-9-(1-hydroxy-2-methylpropyl)-6-(2-iminohexahydro-4-pyrimidinyl)-2-isopropyl-4,7,10-trioxo-3,5,8,11, 15-pentaazaheptadecane-1,17-dioic acid | HCID 178493898 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178446380 | HCID 178446380 | — |
Reaction Steps
To a solution of 50 mg (53 μmol) 16-({[5-(aminomethyl)-4-hydroxy-3-methoxytetrahydro-2-furanyl]oxy}{5-[2,4-dioxo-3,4-dihydro-1 (2H)-pyrimidinyl]-3,4-dihydroxytetrahydro-2-furanyl}methyl)-9-(1-hydroxy-2-methylpropyl)-6-(2-iminohexahydro-4-pyrimidinyl)-2-isopropyl-4,7,10-trioxo-3,5,8,11,15-pentaazaheptadecane-1,17-dioic acid (λmax nm in water=259) in 0.4 ml of methanol is added 9.5 mg (2.0 eq., 110 μmol) of valeraldehyde and 3.3 mg (1.0 eq., 53 μmol) of sodium cyanoborohydride. After stirring for 5 minutes, 0.04 ml of 1 N methanolic hydrochloric acid is added. The reaction mixture is then stirred for 0.5 hour (the reaction is monitored by MS). The solvent is removed under reduced pressure to give a yellow gum. The desired product is identified by LC/MS and separated by preparative HPLC to give 4.9 mg (9.0% yield) of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727232B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-a0bb92e0e61d471fa8acb8da00844869 |
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| Source note | uspto-grants-2004_04 |
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