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HRID 1078093作成日:2026年10月27日

Ammonia → Ninhydrin

https://huagongshe.com/reaction/1078093

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物L-(-)-OrnithineHCID 6262—
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
溶媒DimethylformamideHCID 6228—
溶媒dichloromethane N,N-dimethylformamideHCID 22350042—
生成物NinhydrinHCID 10236—

反応手順

An aminomethyl polystyrene resin support (6.0 g, 0.95 mmol/g, 5.7 mmol) was derivatized with Nα -Fmoc, Nδ -Boc-ornithine by standard procedures. The resin was swollen and washed with dichloromethane, neutralized with 5% DIEA in dichloromethane (1×5 min+3×10 min), and washed with dichloromethane. Coupling of the Orn derivative was mediated by N,N'-diisopropylcarbodiimide (DIPCDI)/HOBt in DMF method (3 equiv. each, 15 min preactivation, 40 mL reaction volume), 3 hours. Washing followed vtth DMF and dichloromethane. A ninhydrin test on a sample was nearly negative, but unreacted sites were blocked by capping with acetic anhydride (4.5 mL, 5 equiv.) and triethylamine (7.0 mL, 5 equiv.) in DMF (20 mL), 30 minutes. The protected Orn-PS resin (0.78 mmol/g, matches theoretical loading as adjusted for expected weight gain) was washed with DMF, dichloromethane, and treated with piperidine-DMF (1:4, v/v) (2+10 min) to remove selectively the Nα -Fmoc group. Further washings with DMF, dichloromethane, 2-propanol, and DMF-dichloromethane (3:7, v/v) prepared the resin for coupling of the MPEG-acid derivative, produced as described in Example 3. A solution of the MPEG-acid (37 g, 18 mmol) in DMF-dichloromethane (3:7 v/v, 75 mL) was combined with HOBt (2.75 g, 18 mmol) and DIPCDI (2.83 mL, 18 mmol) for 15 minutes, and was then added to the H-Orn(Boc)-PS resin. Coupling proceeded for 5 hours giving a slightly positive ninhydrin test. A second coupling with smaller amounts of MPEG-acid derivative and activating agents (9 mmol scale), and acetylation by already-described procedures followed. The final MPEG-Orn(Boc)-PS resin was washed with dichloromethane, DMF, dichloromethane and methanol, and dried in vacuo over P2O5 for 48 hours. There was obtained 16.9 g of resin (excellent agreement with theoretical weight gain) with a loading of 0.31 mmol/g, comprising PEG:PS:Orn=0.57:0.36:0.07 by weight (based on elemental analysis and amino acid analysis). Similar results were obtained when BOP/HOBt/NMM in DMF protocols were used for activation and coupling.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05545698
出典データセットuspto-grants-1996_08
ORD IDord-86cdb561a34e46b4b009fd96c8f35123
出典メモuspto-grants-1996_08