N-(tert-ブトキシカルボニル)-L-プロリン

1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-

HCID 85083

基本情報

CAS
15761-39-4
標準SMILES
CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)O
InChIKey
ZQEBQGAAWMOMAI-ZETCQYMHSA-N
分子式
C10H17NO4
平均分子量
215.25 g/mol
単同位体質量
215.11575802

名称と識別子

優先名称
1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-
IUPAC
(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
現地名
N-(tert-ブトキシカルボニル)-L-プロリン
英語名
BOC-L-Proline
分子式
C10H17NO4
分子量
215.25

名称と別名

Boc-L-prolineN-(tert-Butoxycarbonyl)-L-prolineN-(tert-Butyloxycarbonyl)-L-prolinetert-Butoxycarbonyl-L-proline1-tert-Butoxycarbonyl-L-proline1-tert-Butyloxycarbonyl-L-prolineN-tert-Butoxycarbonylprolinetert-Butyloxycarbonyl-L-prolineNSC 1646601,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-EINECS 239-848-31,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (S)-
名称をさらに表示
N-(tert-ブトキシカルボニル)-L-プロリン(2S)-ピロリジン-1,2-ジカルボン酸1-tert-ブチルN-(tert-ブチルオキシカルボニル)-L-プロリン1-(tert-ブチルオキシカルボニル)-L-プロリン1-(tert-ブトキシカルボニル)プロリン(2S)-1-(tert-ブチルオキシカルボニル)ピロリジン-2-カルボン酸N-Boc-L-プロリン(2S)-ピロリジン-1,2α-ジカルボン酸1-tert-ブチルN-(tert-ブトキシカルボニル)プロリン(2S)-1-(tert-ブチルオキシカルボニル)ピロリジン-2α-カルボン酸(2S)-1-(tert-ブトキシカルボニル)ピロリジン-2-カルボン酸(2S)-1-(tert-ブトキシカルボニル)-ピロリジン-2-カルボン酸ピロリジン-1,2α-ジカルボン酸1-tert-ブチル1-tert-ブトキシカルボニル-L-プロリン1-(tert-ブトキシカルボニル)-L-プロリン(2S)-1,2-ピロリジンジカルボン酸1-tert-ブチルBoc-プロリンBOC-L-プロリンBOC‐L‐プロリンN-T-BOC-L-プロリンBOC-PRO-OH(tert-butoxycarbonyl)-L-prolineBOC-PRON-BOC-L-PROLINE(tert-butoxycarbonyl)prolineBOC-L-PROBOC-L-PRO-OHN-BOC-PROLINE(2S)-1-tert-butoxycarbonylpyrrolidine-2-carboxylic acid
1,2-Pyrrolidinedicarboxylic acid, 1-tert-butyl ester, L-1-(tert-Butyl) hydrogen (S)-pyrrolidine-1,2-dicarboxylateDTXSID00884847RefChem:412214DTXCID5010242681,2-Pyrrolidinedicarboxylic acid, 1-tert-butyl ester, L-(8CI)1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (S)-(9CI)239-848-3

データベース識別子

CAS
15761-39-4
PubChem CID
85083
DTXSID
DTXSID00884847
ChEMBL
CHEMBL1221957
EC Number
239-848-3
Nikkaji
J208.113J

物性

構造計算による物性

XLogP
1.5
極性表面積
66.8 Ų
水素結合供与体数
1
水素結合受容体数
4
回転可能結合数
3
重原子数
15

物理化学的性質

融点
133 · 133-135 °C(lit.)
比旋光度
-60.5 · -60.5 º (c=1, HAc)
沸点
355.52 °C · 355.52°C (rough estimate)
比重(密度)
1.1835 · 1.1835 (rough estimate)
屈折率
-60 ° · -60 ° (C=2, AcOH)
貯蔵温度
Keep in dark place,Sealed in dry,Room Temperature

化学的性質

化学的特性White to off-white microcrystalline powder

安全と法規制

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 75% (6 of 8) of all reports.

Warning

H315 (25%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 8 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesSkin Irrit. 2 (25%)

安全データ

wgk
3
tsca
TSCA listed
hs_code
2933 99 80
risk_code
20/21/22-36/37/38
hazard_code
Xn
safety_code
24/25-36-26

化学と産業

用途と製造

General Manufacturing Information1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-: ACTIVE
応用分野 · 2 件

説明N-Boc-L-proline is a synthetic intermediate. It has been used in the synthesis of enantioselective catalysts for aldol reactions and hepatitis C virus (HCV) NS5A inhibitors.

使用N-Boc-L-proline is used as an intermediate in organic synthesis. It is also used to prepare daclatasvir, which inhibits the hepatitis C virus (HCV) non-structural 5A (NS5A) protein. Further, it is used as a drug in the treatment of hepatitis C virus (HCV).

調製方法 · 1 件

製造方法Triethylamine (16.5 mL, 0.12 mmol) was added dropwise over a period of 10 min to a stirred, ice-cold suspension of l-proline (10.0 g, 8.7 mmol) in dichloromethane (200 mL) in a 500-mL three-necked, round-bottomed flask. A solution of Boc2O (28.3 g, 0.13 mmol) in dichloromethane (100 mL) was then added over a period of 10 min and the mixture was stirred for 2.5 h. Thereafter, 10% aqueous citric acid (50 mL) was added, and the dichloromethane layer was washed with saturated brine (2×50 mL) and with water (50 mL). After drying the organic phase over magnesium sulfate, the solvent was evaporated and the residue was taken up in hot ethyl acetate. Dilution of this solution with hexane gave the product, N-tertbutoxycarbonyl- L-proline (17.8 g, 95%); mp 138–140℃; TLC (silica gel): Rf=0:36 (EtOAc/MeOH, 1:1).

サプライヤー100 社

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
南京一化生物科技有限公司13429882898; 13429882898

関連反応

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