56502-01-3

基本信息
2-[(2S)-(1-叔丁氧羰基)吡咯烷-2-基]乙酸
BOC-L-BETA-高脯氨酸
BOC-BETA-HOMOPROLINE
BOC-BETA-HOMOPRO-OH
BOC-BETA-HOPRO-OH
BOC-L-BETA-HOMOPROLINE
BOC-PRO-(C*CH2)OH
N-BETA-T-BUTOXYCARBONYL-L-BETA-HOMOPROLINE
N-BOC-(2S)-PYRR(2-CHCOOH)
(S)-2-(1-BOC-2-PYRROLIDINYL)ACETIC ACID
(S)-N-T-BUTOXYCARBONYL-PYRROLIDINE-2-ACETIC ACID
Boc-L-beta(3)-homoproline
Boc-L-b-homoproline
boc-β3-homopro-oh
BOC-B-HOMOPROLINE
Boc-L-β-Homo-Pro-OH
Boc-L-beta-HPro-OH
N-beta-(t-Butyloxycarbonyl)-L-homoproline, (S)-N-t-Butyloxycarbonyl-2-(pyrrolidin-2-yl)acetic acid
Boc-b-HoPro-OH
2-[(2S)-(1-tert-Butoxycarbonyl)pyrrolidin-2-yl]acetic acid
(S)-2-(1-Boc-2-pyrrolidinyl)acetic acid, Boc-L-β3-homoproline
物理化學(xué)性質(zhì)
制備方法

88790-37-8

56502-01-3
以 (S)-2-(2-吡咯烷基)乙酸甲酯為原料合成 (S)-2-(1-叔丁氧羰基-2-吡咯烷基)乙酸的一般步驟:將 (2S)-2-(2-甲氧基-2-氧代乙基)-1-吡咯烷羧酸叔丁酯(8.35 g,34.3 mmol)溶于150 mL甲醇中。加入50 mL 1M氫氧化鈉水溶液,將反應(yīng)混合物在室溫下攪拌過夜。反應(yīng)完成后,將溶液在減壓下濃縮至約100 mL。將濃縮后的溶液加入300 mL水中,用乙醚萃取兩次(2×100 mL)。用12N鹽酸將水相酸化至pH 2,再用乙醚萃取兩次(2×100 mL)。將水層用飽和氯化鈉溶液飽和后,用乙醚進(jìn)行第三次萃?。?00 mL)。合并所有有機(jī)層,依次用水和飽和氯化鈉溶液洗滌,然后用無水硫酸鎂干燥。過濾除去干燥劑,濾液在減壓下濃縮,得到標(biāo)題化合物 (S)-2-(1-叔丁氧羰基-2-吡咯烷基)乙酸,為白色固體(7.28 g,31.7 mmol,收率92.6%)。產(chǎn)物經(jīng)1H NMR(300 MHz,CDCl3,旋轉(zhuǎn)異構(gòu)體混合物)確認(rèn):δ 4.16(寬單峰,1H),3.37(寬單峰,2H),3.0-2.8(寬單峰,1H),2.36(雙雙重峰,J = 9.3, 15.3 Hz,1H),2.2-2.0(多重峰,1H),1.9-1.7(多重峰,4H),1.48(單峰,9H)ppm。
參考文獻(xiàn):
[1] Patent: WO2003/76440, 2003, A1. Location in patent: Page/Page column 140
[2] Journal of Organic Chemistry, 2005, vol. 70, # 22, p. 8730 - 8733
[3] Organic and Biomolecular Chemistry, 2003, vol. 1, # 22, p. 3977 - 3988
[4] Tetrahedron Letters, 1997, vol. 38, # 20, p. 3609 - 3610