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Chemical Structure| 109953-95-9 Chemical Structure| 109953-95-9
Chemical Structure| 109953-95-9

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tert-Butyl (2S,4R)-4-(benzyloxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate

CAS No.: 109953-95-9

,98%

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Cat. No.: A1648703 Purity: 98%

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    Product Details of [ 109953-95-9 ]

    CAS No. :109953-95-9
    Formula : C17H25NO4
    M.W : 307.38
    SMILES Code : O=C(N1[C@H](CO)C[C@@H](OCC2=CC=CC=C2)C1)OC(C)(C)C

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    Application In Synthesis of [ 109953-95-9 ]

    * All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

    • Downstream synthetic route of [ 109953-95-9 ]

    [ 109953-95-9 ] Synthesis Path-Downstream   1~1

    • 1
    • [ 40350-83-2 ]
    • [ 109953-95-9 ]
    YieldReaction ConditionsOperation in experiment
    100% 32A. (2S,4R)-tert-butyl 4-(benzyloxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate To a solution of <strong>[40350-83-2](2S,4R)-4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid</strong> (1.00 g, 3.11 mmol) in tetrahydrofuran (10 mL) at -10 C. (ice water-brine) was added N-methyl morpholine (0.359 mL, 3.27 mmol). To this solution was added slowly isobutyl chloroformate (0.429 mL, 3.27 mmol). After 30 min, the mixture was filtered and added to a solution of NaBH4 (0.247 g, 6.53 mmol) in water (1.5 mL) at 0 C. After 30 min, the reaction was quenched via addition of NH4Cl (sat.). The resulting mixture was extracted with EtOAc, and the combined organic layer was washed with brine, dried and concentrated to give 1.12 g colorless oil. Purification via silica gel chromatography gave 32A (colorless oil, 1.04 g, 3.38 mmol, 109% yield). LC-MS Anal. Calc'd for C17H25NO4: 307.18. found [M-Boc+H] 208.0. 1H NMR (400 MHz, chloroform-d) delta ppm 7.27-7.39 (5H, m), 4.91 (1H, d, J=7.1 Hz), 4.47-4.55 (2H, m), 4.05 (1H, br. s.), 3.60-3.76 (2H, m), 3.51-3.59 (1H, m), 3.41 (1H, dd, J=12.1, 4.4 Hz), 2.19 (1H, dd, J=13.7, 7.1 Hz), 1.57-1.69 (1H, m), 1.52 (1H, d, J=7.7 Hz), 1.47 (9 H, s).
    97% With borane-THF; In tetrahydrofuran; at 0 - 20℃; for 3.5h; EXAMPLE 85; Step 1; (2S,4R)-4-Benzyloxy-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester; (2S,4R)-4-Benzyloxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (960 mg, 3 mmol) in THF (5 mL) was cooled to 0 C. using ice-water bath. Then 1M solution of BH3 (6 mL, 6 mmol) in THF was added under nitrogen over period of 30 min. Reaction was stirred at 0 C. for 2 h and at rt for another 1 h. Reaction mixture was poured over ice water and product was extracted with EtOAc. Organic layers were combined, washed with water, brine, saturated sodium bicarbonate, dried over anhydrous MgSO4 and concentrated to give the crude product. It was used in next step without purification (900 mg, 97%).; EXAMPLE 86; Step 1; (2S,4R)-4-Benzyloxy-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert butyl ester; (2S,4R)-4-Benzyloxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (960 mg, 3 mmol) in THF (5 mL) was cooled to 0 C. using ice-water bath. Then 1M solution of BH3 (6 mL, 6 mmol) in THF was added under nitrogen over period of 30 min. Reaction was stirred at 0 C. for 2 h and at rt for another 1 h. Reaction mixture was poured over ice water and product was extracted with EtOAc. Organic layers were combined, washed with water, brine, saturated sodium bicarbonate, dried over anhydrous MgSO4 and concentrated to give the crude product. It was used in next step without purification (900 mg, 97%); MS; m/z 286.2 (M+H); 1H NMR (400 MHz, DMSO-d6); delta 1.90 (m, 1H), 3.09(m, 1H), 4.12(m, 2H), 4.27(m, 1H), 5.46(br s, 2H), 6.92 (d, J=6.8 Hz, 2H), 7.02(s, 4H), 7.08(t, J=5.6 Hz, 1H), 7.35(m, 2H), 9.09(br s, 1H), 9.62(br s, 3H);
    82% To a solution of <strong>[40350-83-2](2S,4R)-4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid</strong> (5.00 g, 15.56 mmol) in tetrahydrofuran (50 mL) at -10 C. was added N-methylmorpholine (1.882 mL, 17.11 mmol). To this solution was added slowly isobutyl chloroformate (2.34 g, 2.25 mL, 17.11 mmol). The resulting mixture was stirred for 30 minutes and filtered, and the filtrate was added to a solution of sodium borohydride (1.18 g, 31.1 mmol) in water (1.5 mL) at 0 C. The resulting mixture was stirred at 0 C. for 30 minutes, and the reaction was quenched by the addition of a saturated solution of NH4Cl. The mixture was extracted with ethyl acetate, and the organic extract was washed with brine, dried with MgSO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using a solvent gradient of 0-2% methanol in dichloromethane to give the title compound as a colorless oil (3.93 g, 82%). 1H NMR (400 MHz, pyridine-d5, 90 C.) delta ppm 7.36 (d, J=7.4 Hz, 2H), 7.30 (t, J=7.3 Hz, 2H), 7.23 (t, J=7.2 Hz, 1H), 4.50 (s, 2H), 4.20-4.29 (m, 2H), 3.92-4.00 (m, 1H), 3.80-3.87 (m, 2H), 3.50-3.59 (m, 1H), 2.16-2.30 (m, 2H), 1.47 (s, 9H)
    Example 45: Synthesis of (2R,4S)-4-[(3,5-bis-trifluoromethyl-benzyl)-(5-bromo- pyrimidin-2-yl)-amino]-2-ethyl-pyrrolidine-1-carboxylic acid tert-butyl ester; To a solution of (2S,4R)-4-benzyloxy-pyrrolidine-1 ,2-dicarboxylic acid 1-ferf-butyl ester (77.8 mmol; 25.O g) in THF (135 mL) is added 0.93 M THF solution of borane THF complex (116.7 mmol; 125 mL) at 0 0C under nitrogen. The solution is stirred for 1.5 hours at room temperature, quenched by dropwise addition of 40 ml of MeOH. After concentrating, the mixture is diluted with 400 ml of dichloromethane and 250 ml of saturated aqueous ammonium chloride solution. The product is extracted twice with 100 ml of dichloromethane. The combined organic layer is washed with 250 ml of brine, dried over MgSO4, filtered, concentrated under reduced pressure to give the crude product (24.3 g).
    16.3 g With BH3*DMS; In tetrahydrofuran; at 0 - 20℃; The Boc-protected L-Hyp 3 was dissolved in THF (100mL) and then cannulated into a slurry of NaH (60% inmineral oil, 11.2 g, 155 mmol) in THF (200 mL) at 0 C.Benzyl bromide (15.0 g, 87.7 mmol) was added dropwise tothe reaction mixture. The flask was warmed to room temperatureand then the mixture was heated under reflux for 6h. The reaction mixture was cooled to room temperature andpoured over ice. The organic solvent was evaporated underreduced pressure and the aqueous solution was washed withEtOAc. The aqueous phase was acidified with 2N HCl untilthe pH was 2, and then it was extracted with EtOAc. Theorganic phase was concentrated under reduced pressure toyield 4 as a brownish yellow oil. This brownish yellow oilwas dissolved in dry THF (300 mL) and cooled to 0 C.BH3·DMS (5.7 mL, 58 mmol) was added dropwise to thereaction mixture, which was then kept stirring at 0 C for anadditional 1 h. The flask was removed from the ice bath, andthe mixture stirred overnight at room temperature. Thereaction mixture was poured over ice and sequentiallyextracted with EtOAc, washed with saturated aqueousNaHCO3, washed with brine, and dried (Na2SO4). Thesolution was concentrated under reduced pressure andpurified through flash column chromatography (FCC; gradientEtOAc/hexanes, from 30 to 50%) to yield 5 [26] as aslightly yellow oil (16.3 g, 70% over three steps).

     

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