CN100503610C - Benzoporphyrin chlorophyll photosensitizer and its preparation process and use - Google Patents
Benzoporphyrin chlorophyll photosensitizer and its preparation process and use Download PDFInfo
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- CN100503610C CN100503610C CNB2006100242010A CN200610024201A CN100503610C CN 100503610 C CN100503610 C CN 100503610C CN B2006100242010 A CNB2006100242010 A CN B2006100242010A CN 200610024201 A CN200610024201 A CN 200610024201A CN 100503610 C CN100503610 C CN 100503610C
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Abstract
The invention relates to a group of novel chlorine family photosensitizer of benzoporphyrin compounds, the method for preparation and use thereof. The compounds have a general formula (I), wherein R1 represents H, CH3, CO2CH3, CH2CO2CH3, CHCO2CH3, R2 represents COOCH3, CO, when R2 is CO, R1 is CHCOOCH3, R3 represents H, low level alkyl, (CH2)mOH, (CH2)mNR4R5, R4 and R5 separately represent low grade alkyl, m represents an integer in the range of 2-6, the low grade alkyl means C1-6 straight chain or branched chain alkyl.
Description
Technical field
The present invention relates to medical technical field, is a kind of novel dihydro porphin photosensitizer---green porphyrins of benzo leaf and its production and use.
Background technology
(photodynamic therapy PDT) is the treatment malignant tumour new technology that grows up the beginning of the eighties to optical dynamic therapy.Its treatment basis is: taken in the tumor tissues of photosensitizers with the photoirradiation selectivity of certain wavelength, brought out photodynamic reaction by photosensitizers, deactivation causes tumor tissue necrosis and brings into play therapeutic action to tumour cell generation cell toxicant.
First-generation Porphyrin-Based Sensitizer such as hematoporphyrin derivative (hematoporphyrin derivative, HpD), phytochrome II (Photofrin II, trade(brand)name: porfimer sodium, Porfimer Sodium), cancer light quinoline (Photocarcinorin, PSD-007) etc. have following shortcoming: (1) is complicated mixing porphyrin preparation, difficult quality control; (2) red light district (〉 600nm) (ε) is little for uptake factor, causes target focus photodynamic effect lowly, has limited the raising of curative effect; (3) high the reaching in vivo of photosensitization porphyrin content of tumour non-selectivity positioning action removed slowly, cause the phototoxicity of healthy tissues big.
A new generation dihydro porphin photosensitizer such as benzoporphyrin derivative (benzoporphyrin derivative, BPD) and chlorophyll a degraded derivative etc., because they have red light district (〉 600nm) maximum absorption wavelength (λ
Max), photosensitization high than Porphyrin-Based Sensitizer red shift and uptake factor (ε) by force and remove advantage such as fast in vivo and overcome the focus that becomes tumour PDT new drug research field substantially.Wherein, benzoporphyrin list acid ring A (BPD-MA, trade(brand)name: Verteporfin, Visudyne) by the exploitation of Canadian QLT Phototherapeutics Inc., get permission to be used for the clinical PDT treatment of tumour and macula retinae sex change in the U.S. in calendar year 2001, the synthetic route of BPD-MA such as accompanying drawing 1 (see Pangka VS et al.J Org Chem for details, 1986,51:1094.).
Because the starting raw material of preparation BPD-MA is protoporphyrin IX dimethyl ester (protoporphyrin IX dimethylester), 3-position on its ring A and the 8-position on the ring B are vinyl, when with dimethyl butyn (dimethyl acetylenedicarboxylate, lack selectivity when DMAD) carrying out the Diels-Alder cycloaddition reaction, therefore, generation is the equal amount of mixture of ring A and two kinds of adducts of ring B.And preparation used during BPD-MA be ring A adduct, so must be after the column chromatography separation obtains encircling the A adduct with two kinds of adducts, to encircle the A adduct more successively through triethylamine (TEA) and 1,8-diazabicyclo [5,4,0] 11-5-alkene (1,8-Diazabicyclo[5,4,0] undec-7-ene DBU) resets and hydrochloric acid hydrolysis makes BPD-MA.
Summary of the invention
The invention provides the novel dihydro porphin photosensitizer that a kind of raw material sources are wide, the preparation method is simple, toxicity is low---the green porphyrins of benzo leaf (benzochloroporphyrin derivatives, BCPD) and and preparation method thereof.
The present invention is raw materials used to be chlorophyll alpha degraded product chlorin e
6(chlorin e
6), chlorin e
4(chlorin e
4), C.I. Natural Red 8-18 (purpurin-18), chlorin p
6(chlorin p
6) and chlorin f (chlorin f), its chemical structural formula is as follows:
Therefore only encircling in their structure has vinyl on the A, can carry out directed Diels-Alder cycloaddition reaction with DMAD, and synthetic what obtain is the ring A adduct of new texture type---the green porphyrins of benzo leaf (BCPD).
Above-mentioned raw materials can be with the chlorophyll a in the silkworm excrement through soda acid degraded preparation.China is world silk big producing country, and silkworm excrement (tame silkworm faeces) is one of main by product of silkworm industry.Can produce 1,000,000 tons of silkworm excrements approximately in the annual silk production of China.Chlorophyll a content accounts for 0.75% in the silkworm excrement, is very abundant and cheap chlorophyll resource.Utilize silkworm excrement to prepare BCPD, can realize the comprehensive utilization of resource, " turning waste into wealth " helps environmental protection.
The compounds of this invention BCPD structure is shown in general formula (I):
Wherein, R
1Represent H, CH
3, COOCH
3, CH
2COOCH
3,-CHCOOCH
3
R
2Represent COOCH
3,-CO works as R
2During for CO and R
1Be CHCOOCH
3Form 5 yuan of rings;
R
3Represent H, low alkyl group, (CH
2)
mOH or (CH
2)
mNR
4R
5, R
4And R
5Represent low alkyl group independently, m represents the integer between the 2-6, and low alkyl group refers to contain the straight or branched alkyl of 1-6 carbon atom.
The compounds of this invention is with silkworm excrement chlorophyll crude extract---and commercially available chlorophyll paste serves as that the base beginning preparation method of raw material is as follows:
1. (chlorophyll is the feedstock production compound VI a), comprises chlorin f (chlorin f, VI with chlorophyll a
1), chlorin p6 (chlorin p
6, VI
2), chlorin e
6(chlorin e
6, VI
3) and chlorin e
4(chlorin e
4, VI
4) [seeing patent CN99119879.4, herbal medicine for details, 1999,30 (80): 568., Chinese Pharmaceutical Journal, 1999,34 (12): 846., Chinese Journal of Pharmaceuticals, 2000,31 (5): 215.], reaction process is seen accompanying drawing 2.
2. prepare the green porphyrins I of target compound benzo leaf with compound VI, reaction process is seen accompanying drawing 3.
Among Fig. 3:
When R is H, R '=R
1=H, R
2=CO
2CH
3, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
When R is CO
2During H, R '=R
1=CO
2CH
3, R
2=CO
2CH
3, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5:
When R is CH
2CO
2During H, R '=CH
2CO
2CH
3, R
1=CH
2CO
2CH
3, CHCO
2CH
3, R
2=CO
2CH
3,-CO works as R
2During for CO and R
1Be CHCOOCH
3Form 5 yuan of rings, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
When R is CH
3The time, R '=R
1=CH
3, R
2=CO
2CH
3, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
R
4And R
5Represent low alkyl group independently;
M represents the integer between the 2-6; Described low alkyl group is meant the straight or branched alkyl that contains 1-6 carbon atom.
The corresponding group of part intermediate compound and target compound is as follows:
Concrete synthesis step is:
1. at first (chlorophyll is that (pheophorbide a), pheophorbide acid a prepares chlorin f (VI to the feedstock production pheophorbide acid a respectively again a) with chlorophyll a
1), chlorin p
6(VI
2), chlorin e
6(VI
3) and chlorin e
4(VI
4):
(1) (pheophorbide a) for the preparation pheophorbide acid a
The diethyl ether solution of commercially available chlorophyll paste generates pheophorbide acid a through concentrated hydrochloric acid stirring reaction 2h under less than 10 ℃ cold condition;
(2) preparation chlorin f (chlorin f, VI
1)
Pheophorbide acid a and 25% potassium hydroxide ethanol liquid, logical O under 0 ℃ of condition
2Behind the reaction 1h, logical again N
2Back flow reaction 0.5h generates VI rapidly
1
(3) preparation chlorin p
6(chlorin p
6, VI
2)
Pheophorbide acid a ether solution and 25% potassium hydroxide n-propyl alcohol liquid, logical O under 0 ℃ of condition
2Reaction 2h generates C.I. Natural Red 8-18 (purpurin-18), and C.I. Natural Red 8-18 is in alkaline aqueous solution, and its hexa-atomic inner-acid anhydride ring splits voluntarily and quantitatively is transformed into VI
2
(4) preparation chlorin e
6(chlorin e
6, VI
3) and chlorin e
4(chlorin e
4, VI
4)
Pheophorbide acid a and 25% potassium hydroxide ethanol liquid are at logical N
2Following back flow reaction 1h generates VI
3Again with VI
3Back flow reaction 1h generates VI in pyridine
4
2. respectively by compound VI
1, VI
2, VI
3, VI
4Preparation benzo leaf green porphyrin class target compound (I):
(1) preparation chlorin f dimethyl ester (V
1), chlorin p
6Trimethyl (V
2), chlorin e
6Trimethyl (V
3) and chlorin e
4Dimethyl ester (V
4):
Respectively with compound VI
1, VI
2, VI
3And VI
4Tetrahydrofuran (THF) (THF) liquid and the diazomethane (CH of 2.8% (w/v)
2N
2) ether solution reaction 10min, promptly get compound V
1, V
2, V
3, V
4
(2) the green porphyrin f of preparation leaf dimethyl ester (IV
1), the green porphyrin p of leaf
6Trimethyl (IV
2), the green porphyrin e of leaf
6Trimethyl (IV
3) and the green porphyrin e of leaf
4Dimethyl ester (IV
4):
Respectively with compound V
1, V
2, V
3And V
4Dichloromethane solution and 2,3-two chloro-5,6-dicyano-1,4-benzoquinones (DDQ) reaction promptly gets compound IV
1, IV
2, IV
3, IV
4
(3) the green porphyrin f of preparation benzo leaf dimethyl ester (III
1), the green porphyrin p of benzo leaf
6Trimethyl (III
2), the green porphyrin e of benzo leaf
6Trimethyl (III
3) and the green porphyrin e of benzo leaf
4Dimethyl ester (III
4):
Respectively with compound IV
1, IV
2, IV
3And IV
4With dimethyl butyn (DMAD) logical N in toluene liquid
2Refluxed 7 days, and carried out the Diels-Alder cycloaddition reaction, promptly get compound III
1, III
2, III
3, III
4
(4) the green porphyrin f of preparation benzo leaf dimethyl ester TEA resets trans-isomer(ide) (II
1), the green porphyrin p of benzo leaf
6Trimethyl TEA resets trans-isomer(ide) (II
2), the green porphyrin e of benzo leaf
6Trimethyl TEA resets trans-isomer(ide) (II
3) and the green porphyrin e of benzo leaf
4Dimethyl ester TEA resets trans-isomer(ide) (II
4):
Respectively with compound III
1, III
2, III
3And III
4Dichloromethane solution and diethylamine (TEA) reaction 4h, promptly get Compound I I
1, II
2, II
3, II
4
(5) the green porphyrin f of preparation target compound benzo leaf dimethyl ester DBU resets cis-isomeride (I
1), the green porphyrin p of benzo leaf
6Trimethyl DBU resets cis-isomeride (I
2), the green porphyrin e of benzo leaf
6Trimethyl DBU resets cis-isomeride (I
3), the green porphyrin e of benzo leaf
4Dimethyl ester DBU resets cis-isomeride (I4) and the green porphyrin e of benzo leaf
6Trimethyl DBU resets and Dickman condensation cis-isomeride (I5):
Respectively with Compound I I
1, II
2And II
4Dichloromethane solution and DBU room temperature reaction 30min, promptly get target compound I
1, I
2, I
4Compound I I
3Dichloromethane solution and DBU room temperature reaction 4h, promptly get target compound I
3, I
5
(6) the green porphyrin f of preparation target compound benzo leaf mono-methyl DBU resets cis-isomeride (I
6), the green porphyrin p of benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
7), the green porphyrin e of benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
8), the green porphyrin e of benzo leaf
4Mono-methyl DBU resets cis-isomeride (I
9), and the green porphyrin e of benzo leaf
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride (I
10):
Respectively with Compound I
1, I
2, I
3, I
4And I
5Through the reaction of 25% hydrochloric acid directionally hydrolyzing, promptly get target compound I
6, I
7, I
8, I
9, I
10
(7) the green porphyrin target compound of preparation benzo leaf I
11, I
12, I
13, I
14, I
15, I
16, I
17, I
18, I
19, I
20
Respectively with Compound I
6, I
7, I
8, I
9And I
10Dichloromethane solution and corresponding substituted alcohols (R
3OH), reaction promptly gets target compound I under dicyclohexylurea (DCU) (DCC) existence condition
11, I
12, I
13, I
14, I
15, I
16, I
17, I
18, I
19, I
20
Description of drawings
Fig. 1 is the synthetic route chart of BPD-MA.Fig. 2 is for being the reacting flow chart of feedstock production compound VI with the chlorophyll a.Fig. 3 is for preparing the reacting flow chart of the green porphyrins I of compound benzo leaf with compound VI.
Embodiment
Below in conjunction with embodiment, the present invention is described in detail, but the following example should not regarded limitation of the scope of the invention as.
Embodiment 1 chlorin f dimethyl ester (V
1) preparation
Get chlorin f (VI
1) 0.65g (1.21mmol) is dissolved in 50mL and heavily steams tetrahydrofuran (THF) (THF), in 0 ℃ of 2.8% (w/v) diazomethane ether solution 10mL (6.67mmol) that adds prepared fresh down, reaction 10mim, the diazomethane that adds 0.2mL glacial acetic acid decomposing excessive then, the THF of reclaim under reduced pressure 2/3 amount adds the dilution of 50mL chloroform, be washed to neutrality, anhydrous sodium sulfate drying reclaims solvent, drying after the silica gel H column chromatography separate black powder V
10.45g, 211～212 ℃ of fusing points, yield 66.2%.UVλ
max(CH
2Cl
2)nm：666(7.1×10
4)，610(7.3×10
3)，529(6.2×10
3)，499(1.7×10
4)，401(1.9×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:9.82,9.77,9.63and 8.75 (each s, each 1H, 4 * meso-H), 8.07 (dd, 1H, J=17.9 and 11.5Hz, 2a-H
x), 6.33 (d, 1H, J=17.9Hz, 2b-H
B), 6.15 (d, 1H, J=11.5Hz, 2b-H
A), 4.50 (m, 2H, 7,8-H), 4.35,3.82,3.62,3.47 and 3.31 (each s, each 3H, 5-, 1-, 3-Me and OMe * 2), 3.77 (q, 2H, J=7.7Hz, 4a-CH
2), 2.74～2.37 (m, 4H, 7a-and 7b-CH
2), 1.88 (d, 3H, J=7.2Hz, 8-Me), 1.72 (t, 3H, J=7.7Hz, 4b-Me) ,-1.67 (br s, 2H, NH in the ring * 2).
Embodiment 2 chlorin p
6Trimethyl (V
2) preparation
2.0g C.I. Natural Red 8-18 (3.55mmol) is dissolved in the 50mL tetrahydrofuran (THF), adds 200mL methyl alcohol and 250mL20% (w/v) aqueous sodium hydroxide solution, stirring at room is reacted to the disappearance of 698nm place ultraviolet absorption peak, needs 1h approximately.Add water 500mL dilution then, be neutralized to pH5～6, ether (200mL * 3) extraction, anhydrous sodium sulfate drying with 10% (w/v) sulfuric acid.Ether solution is bathed under the cooling at cryosel and is added 2.8% (w/v) diazomethane ether solution 30mL (20mmol), and reaction 10mim adds the diazomethane of 0.5mL glacial acetic acid decomposing excessive then, reclaims solvent, drying after the silica gel H column chromatography separate black powder V
21.8g, 232～233 ℃ of fusing points, yield 81.3%.UVλ
max(CH
2Cl
2)nm：669(6.3×10
4)，615(8.2×10
3)，530(9.8×10
3)，499(1.7×10
4)，401(2.1×10
5)(soret)。
1H?NMR(CDCl
3)δ?ppm：9.96，9.38?and8.68(each?s，each?1H，3×meso-H)，7.92(dd，1H，J＝17.9?and?11.5Hz，2a-H
x)，6.28(d，1H，J＝17.9Hz，2b-H
B)，6.10(d，1H，J＝11.5Hz，2b-H
A)，4.46(m，2H，7，8-H)，4.24，4.20，3.88，3.59，3.38?and?3.18(each?s，each?3H，5-，1-，3-Me?and?OMe×3)，3.55(q，2H，J＝7.5Hz，4a-CH
2)，2.51～2.10(m，4H，7a-?and?7b-CH
2)，1.85(d，3H，J＝7.2Hz，8-Me)，1.62(t，3H，J＝7.5Hz，4b-Me)。
Embodiment 3 chlorin e
6Trimethyl (V
3) preparation
According to the method for embodiment 1,3.6g (6.04mmol) chlorin e
6(VI
3) make black solid V with 2.8% (w/v) diazomethane ether solution 40mL (26.67mmol) reaction
32.43g, 209～210 ℃ of fusing points, yield 63.1%.UVλ
max(CH
2Cl
2)nm：664(1.3×10
5)，608(1.5×10
4)，530(1.5×10
4)，501(3.8×10
4)，402(3.7×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:9.69,9.56and 8.75 (each s, each 1H, 3 * meso-H), 8.05 (dd, 1H, J=17.8 and 11.5Hz, 2a-H
x), 6.34 (d, 1H, J=17.8Hz, 2b-H
B), 6.13 (d, 1H, J=11.5Hz, 2b-H
A), 5.34 (d, 1H, J=18.9Hz, 10-H
A), 5.23 (d, 1H, J=18.9Hz, 10-H
B), 4.42 (m, 2H, 7,8-H), 4.25,3.76,3.61,3.57,3.46 and 3.29 (each s, each 3H, 5-, 1-, 3-Me and OMe * 3), 3.79 (q, 2H, J=7.5Hz, 4a-CH
2), 2.54 (m, 2H, 7b-CH
2), 2.18 (m, 2H, 7a-CH
2), 1.75 (d, 3H, J=7.0Hz, 8-Me), 1.70 (t, 3H, J=7.5Hz, 4b-Me) ,-1.28and-1.46 (each br s, each 1H, NH in the ring * 2).
Embodiment 4 chlorin e
4Dimethyl ester (V
4) preparation
According to the method for embodiment 1, chlorin e
4(VI
4) 3.6g (6.52mmol) and 2.8% (w/v) diazomethane ether solution 40mL (26.67mmol) reaction makes black solid V
42.49g, 156～157.5 ℃ of fusing points, yield 63.2%.UVλ
max(CH
2Cl
2)nm：663(6.1×10
4)，607(7.1×10
3)，530(6.7×10
3)，503(1.8×10
4)，404(2.0×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:9.66,9.55and 8.73 (each s, each1H, 3 * meso-H), 8.07 (dd, 1H, J=17.8 and 11.6Hz, 2a-H
x), 6.34 (d, 1H, J=17.8Hz, 2b-H
B), 6.13 (d, 1H, J=11.5Hz, 2b-H
A), 4.45 (m, 2H, 7,8-H), 4.29,3.80,3.61,3.58,3.47 and 3.29 (each s, each 3H, 5-, 1-, 3-Me, meso-γ-Me and OMe * 2), 3.78 (q, 2H, J=7.5Hz, 4a-CH
2), 2.57～1.93 (m, 4H, 7a-CH
2And 7b-CH
2), 1.75 (d, 3H, J=7.2Hz, 8-Me), 1.72 (t, 3H, J=7.5Hz, 4b-Me) ,-1.48 and～1.66 (each br s, each 1H, NH in the ring * 2).
The green porphyrin f of embodiment 5 leaves dimethyl ester (IV
1) preparation
Get chlorin f dimethyl ester (V
1) 0.18g (0.32mmol) is dissolved in the 80mL methylene dichloride, adds the benzole soln 10mL of 75mg (0.33mmol) DDQ, stirring reaction 10min.Reaction solution is used 0.1mol.L successively
-1Hydrochloric acid and water washing, anhydrous sodium sulfate drying reclaims solvent, drying after the silica gel H column chromatography separate brown powder IV
10.17g, yield 95.0%.UVλ
max(CH
2Cl
2)nm：576(9.2×10
3)，552(1.6×10
4)，512(8.9×10
3)，406(1.7×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.93,10.01,9.96 and9.83 (each s, each 1H, 4 * meso-H), 8.16 (dd, 1H, J=17.9 and 11.5Hz, 3
1-H
x), 6.28 (d, 1H, J=17.9Hz, 3
2-HB), 6.13 (d, 1H, J=11.5Hz, 3
2-H
A), 4.44,3.89,3.68,3.58,3.57 and 3.56 (each s, each 3H, 2-, 7-, 12-, 18-Me and13
1-, 17
3-OMe), 4.39 (t, 2H, J=7.8Hz, 17
1-CH
2), 4.03 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.29 (t, 2H, J=7.8Hz, 17
2-CH
2), 1.82 (t, 3H, J=7.6Hz, 8
2-Me) ,-4.12 (br s, 2H, NH in the ring * 2).
The green porphyrin p of embodiment 6 leaves
6Trimethyl (IV
2) preparation
According to the method for embodiment 5,0.13g (0.21mmol) chlorin p
6Trimethyl (V
2) make brown solid IV with 0.07g (0.31mmol) DDQ reaction
20.07g, 231～232 ℃ of fusing points, yield 54.0%.UVλ
max(CH
2Cl
2)nm：549(7.3×10
3)，511(6.0×10
3)，406(1.0×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.01,9.98 and 9.91 (each s, each 1H, 3 * meso-H), 8.08 (dd, 1H, J=17.9 and 11.4Hz, 3
1-H
x), 6.24 (d, 1H, J=17.9Hz, 3
2-HB), 6.10 (d, 1H, J=11.4Hz, 3
2-H
A), 4.45,4.32,3.80,3.67,3.60,3.54 and 3.52 (each s, each 3H, 2-, 7-, 12-, 18-Me and 13
1, 15
1, 17
3-OMe), 4.07 (t, 2H, J=8.5Hz, 17
1-CH
2), 3.99 (q, 2H, J=7.7Hz, 8
1-CH
2), 3.08 (t, 2H, J=8.5Hz, 17
2-CH
2), 1.80 (t, 3H, J=7.7Hz, 8
2-Me) ,-3.78 and-3.82 (each s, each 1H, NH in the ring * 2).
The green porphyrin e of embodiment 7 leaves
6Trimethyl (IV
3) preparation
According to the method for embodiment 5,0.45g (0.71mmol) chlorin e
6Trimethyl (V
3) make brown solid IV with 160mg (0.33mmol) DDQ reaction
30.22g, 240～241 ℃ of fusing points, yield 49.0%.UVλ
max(CH
2Cl
2)nm：578(7.4×10
3)，551(1.0×10
4)，513(1.0×10
4)，409(1.8×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.05,10.04 and 9.93 (each s, each 1H, 3 * meso-H), 8.12 (dd, 1H, J=17.8 and 11.5Hz, 3
1-H
x), 6.28 (dd, 1H, J=17.8 and 1.2Hz, 3
2-HB), 6.10 (dd, 1H, J=11.5 and 1.2Hz, 3
2-H
A), 5.98 (s, 2H, 15
1-CH
2), 4.31,3.79,3.71,3.65,3.63,3.59 and 3.55 (each s, each 3H, 2-, 7-, 12-, 18-Me and 13
1-, 15
2, 17
3-OMe), 4.28 (t, 2H, J=7.2Hz, 17
1-CH
2), 4.05 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.08 (t, 2H, J=7.2Hz, 17
2-CH
2), 1.83 (t, 3H, J=7.6Hz, 8
2-Me) ,-3.06 (br s, 2H, NH in the ring * 2).
The green porphyrin e of embodiment 8 leaves
4Dimethyl ester (IV
4) preparation
According to the method for embodiment 5,1.16g (2.0mmol) chlorin e
4Dimethyl ester (V
4) make brown solid IV with 0.45g (2.0mmol) DDQ reaction
40.69g, fusing point〉and 300 ℃, yield 59.7%.UVλ
max(CH
2Cl
2)nm：670(7.5×10
3)，583(8.5×10
3)，552(1.2×10
4)，514(1.3×10
4)，410(2.1×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:9.97,9.90 and 9.86 (each s, each 1H, 3 * meso-H), 8.12 (dd, 1H, J=17.8 and 11.5Hz, 3
1-H
x), 6.27 (dd, 1H, J=17.8 and 1.3Hz, 3
2-H
B), 6.09 (dd, 1H, J=11.5 and 1.3Hz, 3
2-H
A), 5.98 (s, 2H, 15
1-CH
2), 4.41,4.31,3.80,3.64,3.61,3.57 and 3.54 (each s, each 3H, 2-, 7-, 12-, 18-Me and 13
1, 15-, 17
3-OMe), 4.39 (t, 2H, J=7.5Hz, 17
1-CH
2), 4.04 (q, 2H, J=7.7Hz, 8
1-CH
2), 3.11 (t, 2H, J=7.5Hz, 17
2-CH
2), 1.83 (t, 3H, J=7.7Hz, 8
2-Me) ,-3.09 and-3.15 (each br s, each 1H, NH in the ring * 2).
The green porphyrin f of embodiment 9 benzo leaves dimethyl ester (III
1) preparation
Get the green porphyrin f of leaf dimethyl ester (IV
1) 0.17g (0.3mmol), add toluene 60mL and dimethyl butyn (DMAD) 1.5mL (12.2mmol), logical nitrogen stirring and refluxing reaction 7d reclaims solvent, through the silica gel H column chromatography separate brown powder III
10.10g, 244～245 ℃ of fusing points, yield 47.6%.UVλ
max(CH
2Cl
2)nm：646(5.2×10
4)，590(1.7×10
4)，556(4.8×10
4)，414(4.9×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.76,9.76,9.23 and 9.01 (each s, each 1H, 4 * meso-H), 7.41 (m, 1H, 3
1-H), 4.35,4.02,3.91,3.75,3.71,3.47 and 3.41 (each s, each 3H, 7-, 12-, 18-Me and OMe * 4), 4.32 (t, 2H, J=7.8Hz, 17
1-CH
2), 3.92 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.62 (m, 2H, 3
2-CH
2), 3.27 (t, 2H, J=7.8Hz, 17
2-CH
2), 2.08 (s, 3H, 2-Me), 1.77 (t, 3H, J=7.6Hz, 8
2-Me) ,-2.26 and-2.30 (each br s, each1H, NH in the ring * 2).MS(ESI
+)m/z：707(M+1)(100％)，1413(2M+1)(4％)。
The green porphyrin p of embodiment 10 benzo leaves
6Trimethyl (III
2) preparation
According to the method for embodiment 9, the green porphyrin p of 0.31g (0.50mmol) leaf
6Trimethyl (IV
2) make brown powder III with 3.0mL (24.2mmol) DMAD reaction
20.165g, 245～246 ℃ of fusing points, yield 43.4%.UVλ
max(CH
2Cl
2)nm：655(2.0×10
4)，600(4.6×10
3)，550(1.1×10
4)，519(9.0×10
3)，413(1.5×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.74,9.26 and 9.16 (eachs, each 1H, 3 * meso-H), 7.39 (m, 1H, 3
1-H), 4.37,4.23,3.96,3.90,3.81,3.52,3.45 and 3.42 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 4.05 (m, 2H, 17
1-CH
2), 3.94 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.60 (m, 2H, 3
2-CH
2), 3.02 (m, 2H, 17
2-CH
2), 2.13 (s, 3H, 2-Me), 1.76 (t, 3H, J=7.6Hz, 8
2-Me) ,-2.15 and-2.60 (each br s, each1H, NH in the ring * 2).MS(ESI
+)m/z：765(M+1)(100％)，1529(2M+1)(5％)。
The green porphyrin e of embodiment 11 benzo leaves
6Trimethyl (III
3) preparation
According to the method for embodiment 9, the green porphyrin e of 0.25g (0.39mmol) leaf
6Trimethyl (IV
3) make brown powder III with 2.4mL (19.4mmol) DMAD reaction
30.125g, 225～226 ℃ of fusing points, yield 40.9%.UVλ
max(CH
2Cl
2)nm：653(7.2×10
3)，597(2.4×10
3)，552(4.2×10
3)，521(3.9×10
3)，416(6.7×10
4)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:9.67,9.13 and 9.04 (eachs, each 1H, 3 * meso-H), 7.36 (m, 1H, 3
1-H), 5.76 (s, 2H, 15
1-CH
2), 4.22,3.96,3.90,3.79,3.70,3.46,3.45 and3.39 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 4.15 (t, 2H, J=8.2Hz, 17
1-CH
2), 3.93 (q, 2H, J=7.7Hz, 8
1-CH
2), 3.60 (m, 2H, 3
2-CH
2), 3.00 (t, 2H, J=8.2Hz, 17
2-CH
2), 2.10 (s, 3H, 2-Me), 1.76 (t, 3H, J=7.7Hz, 8
2-Me) ,-1.41 and-2.13 (each br s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：779(M+1)(100％)。
The green porphyrin e of embodiment 12 benzo leaves
4Dimethyl ester (III
4) preparation
According to the method for embodiment 9, the green porphyrin e of 0.29g (0.50mmol) leaf
4Dimethyl ester (IV
4) make brown powder III with 3.0mL (24.2mmol) DMAD reaction
40.13g, 251～252 ℃ of fusing points, yield 36.1%.UVλ
max(CH
2Cl
2)nm：653(2.2×10
4)，597(7.6×10
3)，554(1.3×10
4)，521(1.3×10
4)，416(2.4×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.58,9.05 and 8.93 (eachs, each 1H, 3 * meso-H), 7.34 (m, 1H, 3
1-H), 4.24,4.20,3.96,3.90,3.81,3.47,3.43 and 3.37 (each s, each 3H, 7-, 12-, 18-, 15-Me and OMe * 4), 4.23 (m, 2H, 17
1-CH
2), 3.91 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.61 (m, 2H, 3
2-CH
2), 3.07 (m, 2H, 17
2-CH
2), 2.09 (s, 3H, 2-Me), 1.75 (t, 3H, J=7.6Hz, 8
2-Me) ,-1.33 and-1.92 (each br s, each1H, NH in the ring * 2).MS(ESI
+)m/z：721(M+1)(100％)，1441(2M+1)(4％)。
The green porphyrin f of embodiment 13 benzo leaves dimethyl ester TEA resets trans-isomer(ide) (II
1) preparation
Get the green porphyrin f of benzo leaf dimethyl ester (III
1) 0.12g (0.17mmol), be dissolved in the 80mL methylene dichloride, add 1.6mL triethylamine (TEA), stirring at room reaction 4h reclaims solvent, through the silica gel H column chromatography separate black powder II
10.10g, 241～242 ℃ of fusing points, yield 83.3%.UVλ
max(CH
2Cl
2)nm：663(1.0×10
4)，583(1.8×10
4)，430(7.1×10
4)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.71,9.71,9.09 and 9.08 (each s, each 1H, 4 * meso-H), 7.66 (dd, 1H, J=5.8 and 2.8Hz, 3
2-H), 7.24 (d, 1H, J=5.8Hz, 3
1-H), 4.70 (d, 1H, J=2.8Hz, 2
1-H), 4.36,4.25,3.95,3.74,3.70,3.44 and 3.36 (each s, each 3H, 7-, 12-, 18-Me and 4 * OMe), 4.30 (t, 2H, J=7.8Hz, 17
1-CH
2), 3.90 (q, 2H, J=7.5Hz, 8
1-CH
2), 3.62 (m, 2H, 3
2-CH
2), 3.25 (t, 2H, J=7.8Hz, 17
2-CH
2), 1.75 (t, 3H, J=7.5Hz, 8
2-Me), 1.56 (s, 3H, 2-Me) ,-2.47 and-2.53 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：707(M+1)(100％)，1413(2M+1)(6％)。
The green porphyrin p of embodiment 14 benzo leaves
6Trimethyl TEA resets trans-isomer(ide) (II
2) preparation
According to the method for embodiment 13, the green porphyrin p of 50mg (0.065mmol) benzo leaf
6Trimethyl (III
2) make black powder II with the reaction of 1.0mL triethylamine
250mg, yield 100%.UVλ
max(CH
2Cl
2)nm：670(1.2×10
4)，578(1.9×10
4)，434(8.0×10
4)(soret)。
1HNMR (300Hz, CDCl
3) δ ppm:9.73,9.29 and 9.09 (each s, each 1H, 3 * meso-H), 7.68 (dd, 1H, J=5.9 and 2.8Hz, 3
2-H), 7.24 (d, 1H, J=5.9Hz, 3
1-H), 4.71 (d, 1H, J=2.8Hz, 2
1-H), and 4.39,4.26,4.23,3.94,3.81,3.53,3.46and 3.30 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 3.99～3.91 (m, 4H, 17
1-CH
2And 8
1-CH
2), 3.04 (t, 2H, J=8.4Hz, 17
2-CH
2), 1.75 (t, 3H, J=7.6Hz, 8
2-Me), 1.56 (s, 3H, 2-Me) ,-2.27 and-2.75 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：765(M+1)(100％)，1529(2M+1)(4％)。
The green porphyrin e of embodiment 15 benzo leaves
6Trimethyl TEA resets trans-isomer(ide) (II
3) preparation
According to the method for embodiment 13, the green porphyrin e of 50mg (0.06mmol) benzo leaf
6Trimethyl (III
3) make black powder II with the reaction of 0.8mL triethylamine
350mg, yield 100%.UVλ
max(CH
2Cl
2)nm：668(9.0×10
3)，581(1.4×10
4)，440(7.1×10
4)(soret)。
1HNMR (300Hz, CDCl
3) δ ppm:9.66,9.20 and 8.96 (each s, each1H, 3 * meso-H), 7.65 (dd, 1H, J=5.9 and 2.8Hz, 3
2-H), 7.19 (d, 1H, J=5.9Hz, 3
1-H), 5.77 (s, 2H, 15
1-CH
2), 4.74 (d, 1H, J=2.8Hz, 2
1-H), 4.24,4.22,3.97,3.80,3.72,3.47,3.46 and 3.30 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 4.17 (t, 2H, J=8.3Hz, 17
1-CH
2), 3.90 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.04 (t, 2H, J=8.3Hz, 17
2-CH
2), 1.74 (t, 3H, J=7.6Hz, 8
2-Me), 1.55 (s, 3H, 2-Me) ,-1.50 and-2.24 (each br s, each1H, NH in the ring * 2).MS(ESI
+)m/z：779(M+1)(100％)，1557(2M+1)(3％)。
The green porphyrin e of embodiment 16 benzo leaves
4Dimethyl ester TEA resets trans-isomer(ide) (II
4) preparation
According to the method for embodiment 13, the green porphyrin e of 50mg (0.07mmol) benzo leaf
4Dimethyl ester (III
4) make black powder II with the reaction of 1.0mL triethylamine
450mg, yield 100%.UVλ
max(CH
2Cl
2)nm：670(4.5×10
3)，583(7.9×10
3)，440(3.7×10
4)(soret)。
1HNMR (300Hz, CDCl
3) δ ppm:9.59,9.10 and 8.99 (each s, each 1H, 3 * meso-H), 7.66 (dd, 1H, J=5.9 and 2.8Hz, 3
2-H), 7.24 (d, 1H, J=5.9Hz, 3
1-H), 4.74 (d, 1H, J=2.8Hz, 2
1-H), 4.32 (m, 2H, 17
1-CH
2), 4.28,4.25,4.22,3.94,3.81,3.47,3.44 and 3.33 (each s, each 3H, 7-, 12-, 18-, 15-Me and OMe * 4), 3.89 (q, 2H, J=7.6Hz, 8
1-CH
2), 3.05 (m, 2H, 17
2-CH
2), 1.74 (t, 3H, J=7.6Hz, 8
2-Me), 1.54 (s, 3H, 2-Me) ,-1.44 and-1.98 (eachs, each 1H, NH in the ring * 2).MS(ESI
+)m/z：721(M+1)(100％)，1441(2M+1)(6％)。
The green porphyrin f of embodiment 17 benzo leaves dimethyl ester DBU resets cis-isomeride (I
1) preparation
Get the green porphyrin f of benzo leaf dimethyl ester TEA and reset trans-isomer(ide) (II
1) 0.1g (0.14mmol), be dissolved in the 20mL methylene dichloride, add 0.7mL DBU, stirring reaction 30min, reaction solution use 1mol.L successively
-1Hydrochloric acid, water and saturated common salt water washing, anhydrous sodium sulfate drying reclaims solvent, and drying gets black powder I
10.1g, 248～249 ℃ of fusing points, yield 100%.UVλ
max(CH
2Cl
2)nm：670(3.6×10
4)，592(4.6×10
4)，438(1.6×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.71,9.79,9.28 and 8.88 (each s, each 1H, 4 * meso-H), 7.81 (d, 1H, J=5.7Hz, 3
2-H), 7.43 (d, 1H, J=5.7Hz, 3
1-H), 5.05 (s, 1H, 2
1-H), 4.35,3.99,3.76,3.71,3.46,3.42 and 3.01 (each s, each 3H, 7-, 12-, 18-Me and 4 * OMe), 4.30 (t, 2H, J=7.8Hz, 171-CH
2), 3.95 (q, 2H, J=7.7Hz, 8
1-CH
2), 3.26 (t, 2H, J=7.8Hz, 17
2-CH
2), 1.80 (s, 3H, 2-Me), 1.77 (t, 3H, J=7.7Hz, 8
2-Me) ,-2.03 and-2.07 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：707(M+1)(100％)，1413(2M+1)(6％)。
The green porphyrin p of embodiment 18 benzo leaves
6Trimethyl DBU resets cis-isomeride (I
2) preparation
According to the method for embodiment 17, the green porphyrin p of 95mg (0.124mmol) benzo leaf
6Trimethyl TEA resets trans-isomer(ide) (II
2) make black powder I with the 0.8mLDBU reaction
290mg, yield 94.7%.UVλ
max(CH
2Cl
2)nm：677(2.3×10
4)，586(3.1×104)，439(1.1×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.74,9.30 and 9.02 (each s, each 1H, 3 * meso-H), 7.82 (d, 1H, J=5.7Hz, 3
2-H), 7.44 (d, 1H, J=5.7Hz, 3
1.H), 5.07 (s, 1H, 2
1-H), and 4.36,4.23,3.99,3.80,3.52,3.44,3.39and 3.00 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 3.99～3.91 (m, 4H, 17
1-CH
2And 8
1-CH
2), 3.04 (m, 2H, 17
2-CH
2), 1.79 (s, 3H, 2-Me), 1.75 (t, 3H, J=7.6Hz, 8
2-Me) ,-1.92 and-2.23 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：765(M+1)(100％)。
The green porphyrin e of embodiment 19 benzo leaves
6Trimethyl DBU resets cis-isomeride (I
3) and the green porphyrin e of benzo leaf
6The preparation of trimethyl DBU rearrangement and Dickman condensation cis-isomeride (I5)
According to the method for embodiment 17, the green porphyrin e of 50mg (0.064mmol) benzo leaf
6Trimethyl TEA resets trans-isomer(ide) (II
3) after separating, the silica gel H column chromatography makes black powder I with 0.7mLDBU reaction 4h
3And I
5
I
3(35mg, yield 70%): UV λ
Max(CH
2Cl
2) nm:675 (1.1 * 10
4), 596 (2.2 * 104), 443 (7.7 * 10
4) (soret).
1HNMR (300Hz, CDCl
3) δ ppm:9.92,9.32 and 9.04 (each s, each 1H, 3 * meso-H), 7.82 (d, 1H, J=5.7Hz, 3
2-H), 7.48 (d, 1H, J=5.7Hz, 3
1-H), 6.40 (br d, 2H, 151-CH
2), 5.09 (s, 1H, 2
1-H), 4.30 (m, 2H, 17
1-CH
2), 4.00,3.98,3.93,3.87,3.70,3.48,3.42 and 3.03 (each s, each 3H, 7-, 12-, 18-Me and OMe * 5), 3.95 (q, 2H, J=7.6Hz, 8
1-CH
2), 2.90 (m, 2H, 17
2-CH
2), 1.82 (s, 3H, 2-Me), 1.78 (t, 3H, J=7.6Hz, 8
2-Me) ,-1.26 and-1.81 (each br s, each1H, NH in the ring * 2).MS(ESI
+)m/z：779(M+1)(51％)，801(M+Na)(100％)，817(M+K)(43％)。
I
5(10mg, yield 20%): UV λ
Max(CH
2Cl
2) nm:666 (9.2 * 10
3), 620 (2.2 * 10
4), 444 (7.5 * 10
4) (soret).
1HNMR (300Hz, CDCl
3) δ ppm:9.68,9.20 and 8.78 (each s, each1H, 3 * meso-H), 7.81 (dd, 1H, J=5.7 and 3.0Hz, 3
2-H), 7.48 (d, 1H, J=5.7Hz, 3
1-H), 6.74 (s, 1H, 15
1-CH), 5.04 (d, 1H, J=3.0Hz, 2
1-H), 4.08 (m, 2H, 17
1-CH
2), 4.00,3.81,3.75,3.71,3.40,3.36 and 3.05 (each s, each 3H, 7-, 12-, 18-Me and OMe * 4), 3.88 (m, 2H, 8
1-CH
2), 2.90 (m, 2H, 17
2-CH
2), 1.81 (s, 3H, 2-Me), 1.75 (t, 3H, 8
2-Me) ,-0.60 and-1.50 (each br s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：747(M+1)(100％)，785(M+K)(13％)。
The green porphyrin e of embodiment 20 benzo leaves
4Dimethyl ester DBU resets cis-isomeride (I
4) preparation
According to the method for embodiment 17, the green porphyrin e4 of 80mg (0.11mmol) benzo leaf dimethyl ester TEA resets trans-isomer(ide) (II
4) make black powder I with 0.8mL DBU reaction
465mg, yield 81.3%.UVλ
max(CH
2Cl
2)nm：677(2.7×10
4)，591(3.8×10
4)，451(1.6×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.60,9.10 and 8.79 (each s, each 1H, 3 * meso-H), 7.80 (d, 1H, J=5.8Hz, 3
2-H), 7.39 (d, 1H, J=5.8Hz, 3
1-H), 5.02 (s, 1H, 2
1-H), 4.28 (t, 2H, J=8.2Hz, 17
1-CH
2), 4.23,4.17,3.98,3.81,3.46,3.43,3.36 and 2.99 (each s, each3H, 7-, 12-, 18-, 15-Me and OMe * 4), 3.90 (q, 2H, J=7.5Hz, 8
1-CH
2), 3.06 (t, 2H, J=8.2Hz, 17
2-CH
2), 1.75 (s, 3H, 2-Me), 1.74 (t, 3H, J=7.5Hz, 8
2-Me) ,-1.20and-1.62 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：721(M+1)(100％)，1441(2M+1)(4％)。
The green porphyrin f of embodiment 21 benzo leaves mono-methyl DBU resets cis-isomeride (I
6) preparation
Get the green porphyrin f of benzo leaf dimethyl ester DBU and reset cis-isomeride (I
1) 50mg (0.071mmol), be dissolved in the 15mL tetrahydrofuran (THF), add 25% salt acid liquid 15mL, the TLC monitoring is stirring reaction down.Reaction finishes, the 60mL that adds methylene chloride dilution, water and saturated common salt water washing are to neutral successively, anhydrous sodium sulfate drying reclaims solvent, drying, silica gel H column chromatography separate black powder I
635mg, 268～269 ℃ of fusing points, yield 71.4%.UVλ
max(CH
2Cl
2)mm：670(2.8×10
4)，592(3.5×10
4)，438(1.2×10
5)(soret)。
1H NMR (500Hz, CDCl
3) δ ppm:10.72,9.78,9.30 and 8.91 (each s, each1H, 4 * meso-H), 7.84 (d, 1H, J=5.7Hz, 3
2-H), 7.46 (d, 1H, J=5.7Hz, 3
1-H), 5.08 (s, 1H, 2
1-H), and 4.33,4.01,3.76,3.48,3.43 and 3.03 (each s, each 3H, 7-, 12-, 18-Me and3 * OMe), 4.26 (t, 2H, J=7.8Hz, 17
1-CH
2), 3.92 (q, 2H, J=7.7Hz, 8
1-CH
2), 3.31 (t, 2H, J=7.8Hz, 17
2-CH
2), 1.83 (s, 3H, 2-Me), 1.77 (t, 3H, J=7.7Hz, 8
2-Me) ,-2.03 and-2.08 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：693(M+1)(100％)。
The green porphyrin p of embodiment 22 benzo leaves
6Dimethyl ester DBU resets the preparation of cis-isomeride (I7)
According to the method for embodiment 21, the green porphyrin p of 50mg (0.065mmol) benzo leaf
6Trimethyl DBU resets cis-isomeride (I
2) make black powder I735mg, yield 71.3% with the 15mL25% hydrochloric acid reaction.UVλ
max(CH
2Cl
2)nm：677(1.8×10
4)，588(2.4×10
4)，438(0.9×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.71,9.28 and 9.0 (each s, each 1H, 3 * meso-H), 7.81 (d, 1H, J=5.7Hz, 3
2-H), 7.41 (d, 1H, J=5.7Hz, 3
1-H), 5.05 (s, 1H, 2
1-H), and 4.34,4.21,3.78,3.50,3.41,3.36 and2.99 (each s, each 3H, 7-, 12-, 18-Me and OMe * 4), 3.97～3.88 (m, 4H, 17
1-CH
2And 8
1-CH
2), 3.03 (m, 2H, 17
2-CH
2), 1.78 (s, 3H, 2-Me), 1.74 (t, 3H, J=7.6Hz, 8
2-Me) ,-1.92 and-2.20 (each s, each1H, NH in the ring * 2).MS(ESI
+)m/z：751(M+1)(100％)。
The green porphyrin e of embodiment 23 benzo leaves
6Dimethyl ester DBU resets the preparation of cis-isomeride (I8)
According to the method for embodiment 21, the green porphyrin e of 35mg (0.045mmol) benzo leaf
6Trimethyl DBU resets cis-isomeride (I3) and makes black powder I with the 10mL25% hydrochloric acid reaction
820mg, yield 58.2%.UVλ
max(CH
2Cl
2)nm：675(8.5×10
3)，595(1.7×10
4)，442(5.9×10
4)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.89,9.31 and 9.02 (each s, each 1H, 3 * meso-H), 7.80 (d, 1H, J=5.7Hz, 3
2-H), 7.46 (d, 1H, J=5.7Hz, 3
1-H), 6.39 (br d, 2H, 15
1-CH
2), 5.08 (s, 1H, 2
1-H), 4.28 (m, 2H, 17
1-CH
2), 4.01,3.91,3.85,3.69,3.46,3.39 and 3.01 (each s, each3H, 7-, 12-, 18-Me and OMe * 4), 3.92 (q, 2H, J=7.6Hz, 81-CH
2), 2.91 (m, 2H, 17
2-CH
2), 1.81 (s, 3H, 2-Me), 1.76 (t, 3H, J=7.6Hz, 8
2-Me) ,-1.26and-1.79 (each br s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：765(M+1)(50％)，787(M+Na)(100％)，803(M+K)(40％)。
The green porphyrin e of embodiment 24 benzo leaves
4Mono-methyl DBU resets the preparation of cis-isomeride (I9)
According to the method for embodiment 21, the green porphyrin e of 50mg (0.069mmol) benzo leaf
4Dimethyl ester DBU resets cis-isomeride (I
4) make black powder I with the 15mL25% hydrochloric acid reaction
930mg, yield 61.2%.UVλ
max(CH
2Cl
2)nm：677(2.1×10
4)，590(2.9×10
4)，450(1.2×10
5)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.58,9.09and8.78 (each s, each1H, 3 * meso-H), 7.79 (d, 1H, J=5.8Hz, 3
2-H), 7.38 (d, 1H, J=5.8Hz, 3
1-H), 5.01 (s, 1H, 2
1-H), 4.25 (t, 2H, J=8.2Hz, 17
1-CH
2), 4.21,4.15,3.78,3.43,3.40,3.34 and 2.97 (each s, each 3H, 7-, 12-, 18-, 15-Me and OMe * 3), 3.88 (q, 2H, J=7.5Hz, 8
1-CH
2), 3.04 (t, 2H, J=8.2Hz, 17
2-CH
2), 1.76 (s, 3H, 2-Me), 1.72 (t, 3H, J=7.5Hz, 8
2-Me) ,-1.20 and-1.60 (each s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：707(M+1)(100％)。
The green porphyrin e of embodiment 25 benzo leaves
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride (I
10) preparation
According to the method for embodiment 21, the green porphyrin e of 30mg (0.04mmol) benzo leaf
6Trimethyl DBU resets and Dickman condensation cis-isomeride (I
5) make black powder I with the 10mL25% hydrochloric acid reaction
1015mg, yield 51.0%.UVλ
max(CH
2Cl
2)nm：665(7.1×10
3)，620(1.7×10
4)，443(5.8×10
4)(soret)。
1H NMR (300Hz, CDCl
3) δ ppm:9.66,9.18 and 8.77 (each s, each 1H, 3 * meso-H), 7.80 (dd, 1H, J=5.7 and 3.0Hz, 3
2-H), 7.47 (d, 1H, J=5.7Hz, 3
1-H), 6.71 (s, 1H, 15
1-CH), 5.02 (d, 1H, J=3.0Hz, 2
1-H), 4.10 (m, 2H, 17
1-CH
2), 3.98,3.73,3.69,3.38,3.34 and 3.0 (each s, each 3H, 7-, 12-, 18-Me and OMe * 3), 3.86 (m, 2H, 8
1-CH
2), 2.89 (m, 2H, 17
2-CH
2), 1.80 (s, 3H, 2-Me), 1.75 (t, 3H, 8
2-Me) ,-0.60 and-1.45 (each br s, each 1H, NH in the ring * 2).MS(ESI
+)m/z：733(M+1)(100％)。
The green porphyrin f of embodiment 26 benzo leaves mono-methyl DBU resets cis-isomeride-17-glycol ester (I
11) preparation
Get the green porphyrin f of benzo leaf mono-methyl DBU and reset cis-isomeride (I
6) 50mg (0.072mmol), be dissolved in the 20mL methylene dichloride, add dicyclohexylurea (DCU) (DCC) 50mg, 4-N, N-Dimethylamino pyridine (DMAP) 5mg and ethylene glycol 0.5mL, the TLC monitoring is the stirring at room reaction down.Reaction finishes, and reaction solution adds 60mL dilution, uses dichloromethane extraction (30mL * 3) then, and anhydrous sodium sulfate drying reclaims solvent, drying, silica gel H column chromatography separate black powder I
1130mg, yield 56.4%.UVλ
max(CH
2Cl
2)nm：670(3.1×10
4)，592(3.8×10
4)，438(1.3×10
5)(soret)。MS(ESI
+)m/z：737(M+1)(100％)。
The green porphyrin f of embodiment 27 benzo leaves mono-methyl DBU resets cis-isomeride-17-(2-N, N-dimethylamino) ethanol ester (I
16) preparation
According to the method for embodiment 26, the green porphyrin f of 50mg (0.072mmol) benzo leaf mono-methyl DBU resets cis-isomeride (I
6) dichloromethane solution and 0.5mL2-(N, N-dimethylamino) ethanol, 50mg dicyclohexylurea (DCU) (DCC), 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1635mg, yield 63.5%.UVλ
max(CH
2Cl
2)nm：672(2.9×10
4)，591(3.4×10
4)，439(1.2×10
5)(soret)。MS(ESI
+)m/z：764(M+1)(100％)。
The green porphyrin p of embodiment 28 benzo leaves
6Dimethyl ester DBU resets cis-isomeride-17-glycol ester (I
12) preparation
According to the method for embodiment 26, the green porphyrin p of 50mg (0.067mmol) benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
7) dichloromethane solution and 0.5mL ethylene glycol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1230mg, yield 56.7%.UVλmax(CH
2Cl
2)nm：677(2.1×10
4)，588(2.6×10
4)，438(1.0×10
5)(soret)。MS(ESI
+)m/z：795(M+1)(100％)。
The green porphyrin p of embodiment 29 benzo leaves
6Dimethyl ester DBU resets cis-isomeride-17-(2-N, N-dimethylamino) ethanol ester (I
17) preparation
According to the method for embodiment 26, the green porphyrin p of 50mg (0.067mmol) benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
7) dichloromethane solution and 0.5mL2-(N, N-dimethylamino) ethanol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1735mg, yield 63.9%.UVλ
max(CH
2Cl
2)nm：678(1.9×10
4)，587(2.3×10
4)，439(0.9×10
5)(soret)。MS(ESI
+)m/z：822(M+1)(100％)。
The green porphyrin e of embodiment 30 benzo leaves
6Dimethyl ester DBU resets cis-isomeride-17-glycol ester (I
13) preparation
According to the method for embodiment 26, the green porphyrin e of 50mg (0.065mmol) benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
8) dichloromethane solution and 0.5mL ethylene glycol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1330mg, yield 56.7%.UVλ
max(CH
2Cl
2)nm：675(1.2×10
4)，588(2.0×10
4)，438(0.7×10
5)(soret)。MS(ESI
+)m/z：809(M+1)(55％)，831(M+Na)(100％)，847(M+K)(45％)。
The green porphyrin e of embodiment 31 benzo leaves
6Dimethyl ester DBU resets cis-isomeride-17-(2-N, N-dimethylamino) ethanol ester (I
18) preparation
According to the method for embodiment 26, the green porphyrin e of 50mg (0.065mmol) benzo leaf
6Dimethyl ester DBU resets cis-isomeride (I
8) dichloromethane solution and 0.5mL2-(N, N-dimethylamino) ethanol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1835mg, yield 64.0%.UVλ
max(CH
2Cl
2)nm：676(1.0×10
4)，587(1.6×10
4)，439(0.6×10
5)(soret)。MS(ESI
+)m/z：836(M+1)(50％)，858(M+Na)(100％)，874(M+K)(40％)。
The green porphyrin e of embodiment 32 benzo leaves
4Mono-methyl DBU resets cis-isomeride-17-glycol ester (I
14) preparation
According to the method for embodiment 26, the green porphyrin e of 50mg (0.071mmol) benzo leaf
4Mono-methyl DBU resets cis-isomeride (I
9) dichloromethane solution and 0.5mL ethylene glycol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1430mg, yield 56.5%.UVλ
max(CH
2Cl
2)nm：677(2.4×10
4)，590(3.1×10
4)，450(1.3×10
5)(soret)。MS(ESI
+)m/z：751(M+1)(100％)。
The green porphyrin e of embodiment 33 benzo leaves
4Mono-methyl DBU resets cis-isomeride-17-(2-N, N-dimethylamino) ethanol ester (I
19) preparation
According to the method for embodiment 26, the green porphyrin e of 50mg (0.071mmol) benzo leaf
4Mono-methyl DBU resets cis-isomeride (I
9) dichloromethane solution and 0.5mL2-(N, N-dimethylamino) ethanol, 50mg dicyclohexylurea (DCU) (DCC) and 5mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1935mg, yield 63.6%.UVλ
max(CH
2Cl
2)nm：678(2.2×10
4)，591(2.8×10
4)，450(1.2×10
5)(soret)。MS(ESI
+)m/z：778(M+1)(100％)。
The green porphyrin e of embodiment 34 benzo leaves
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride-17-glycol ester (I
15) preparation
According to the method for embodiment 26, the green porphyrin e of 30mg (0.041mmol) benzo leaf
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride (I
10) dichloromethane solution and 0.3mL ethylene glycol, 30mg dicyclohexylurea (DCU) (DCC) and 3mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
1515mg, yield 47.2%.UVλ
max(CH
2Cl
2)nm：665(1.0×10
4)，620(1.9×10
4)，443(0.7×10
5)(soret)。MS(ESI
+)m/z：777(M+1)(100％)。
The green porphyrin e of embodiment 35 benzo leaves
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride-17-(2-N, N-dimethylamino) ethanol ester (I
20) preparation
According to the method for embodiment 26, the green porphyrin e of 25mg (0.034mmol) benzo leaf
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride (I
10) dichloromethane solution and 0.3mL2-(N, N-dimethylamino) ethanol, 30mg dicyclohexylurea (DCU) (DCC) and 3mg4-N, N-Dimethylamino pyridine (DMAP) reaction makes black powder I
2015mg, yield 54.7%.UVλ
max(CH
2Cl
2)nm：666(0.8×10
4)，619(1.6×10
4)，444(0.6×10
5)(soret)。MS(ESI
+)m/z：804(M+1)(100％)。
The photosensitive anti-tumor activity test of the green porphyrin class of part benzo leaf of the present invention target compound.
1. material
Cell strain is selected BEL7402 (human liver cancer cell) for use, is provided by hemopathy institute of the Chinese Academy of Medical Sciences.
LASER Light Source adopts the 670nm semiconductor laser therapeutic instrument of Nankai University's contemporary optics Research Institute, and peak power output is 2W.
2. method
People's liver cancer BEL7402 cell cultures: from liquid nitrogen, take out freeze-stored cell, place 42 ℃ of water-baths to make cell change the RPMI-1640 that contains fresh calf serum after the dissolving fast immediately, place 37 ℃ of CO
2Cultivate in the incubator, change nutrient solution every other day one time.
The soup preparation: (BPDMA verteporfin) is dissolved in DMSO, is made into 0.5mg.L to get testing compound of the present invention and positive control medicine Visudyne
-1The medicine storage liquid, with the physiological saline dilution that contains DMSO, ultimate density is respectively: 2.5 μ g.mL before the experiment
-1, 2 μ g.mL
-1, 1.5 μ g.mL
-1, 1.0 μ g, mL
-1, 0.5 μ g.mL
-1, 0.25 μ g.mL
-1, 0.125 μ g.mL
-1, 0.0625 μ g.mL
-1, 0.03125 μ g.mL
-1
Dark toxicity and light power lethal effect to people's liver cancer BEL7402 cell are measured: the cell in the vegetative period of taking the logarithm, use 0.25% trysinization, and after stopping digesting, cell concn is adjusted into 1 * 10
4Individual/mL, be inoculated in 96 well culture plates 6 every group multiple holes, every hole 100 μ L.Behind the cell attachment, add the physiological saline diluent of the photosensitizers of different concns in the cell, use Hank ' s liquid to wash 2 times after hatching 4h or 24h, renew bright nutrient solution.With the irradiation of 670nm semiconductor laser, light dosage is 10J.cm
-2, according to finishing, continue to cultivate 24h, repel measuring cytoactive { cell lethality (%)=[dead cell sum/(viable cell sum+dead cell sum)] * 100%} with Yihong dyestuff.
3. result
Part target compound of the present invention is to the dark toxicity result of vitro human liver cancer BEL7402 cell, sees Table 1 and table 2.
Part target compound of the present invention is to the light power lethal effect result of vitro human liver cancer BEL7402 cell, sees Table 3 and table 4.
The single administration of table 1 is not after irradiation is hatched 4h, and reagent is to the lethality rate (unit: %) of vitro human liver cancer BEL7402 cell
Annotate: the simple BEL7402 groups of cells of cell---(not administration and physiological saline), NS---contains the physiological saline of DMSO
The single administration of table 2 is not after irradiation is hatched 24h, and reagent is to the lethality rate (unit: %) of vitro human liver cancer BEL7402 cell
Annotate: the simple BEL7402 groups of cells of cell---(not administration and physiological saline), NS---contains the physiological saline of DMSO
4h back light (light dosage 10J.cm is hatched in table 3 administration
-2), reagent is to the lethality rate (unit: %) of vitro human liver cancer BEL7402 cell
Annotate: the simple BEL7402 groups of cells of cell---(not administration and physiological saline), NS---contains the physiological saline of DMSO
24h back light (light dosage 10J.cm is hatched in table 4 administration
-2) time, reagent is to the lethality rate (unit: %) of vitro human liver cancer BEL7402 cell
Annotate: the simple BEL7402 groups of cells of cell---(not administration and physiological saline), NS---contains the physiological saline of DMSO
Above-mentioned experimental result shows:
(1) it is all very little to be tried the dark toxicity of the green porphyrin class of benzo leaf each concentration of target compound and different incubation time pair cell, illustrates to be tried the green porphyrin class of benzo leaf target compound effect is little to the activity influence of tumour cell separately; And present extremely strong dark toxicity (table 1 and table 2) with the prolongation of itself and cell incubation time as positive control drug BPDMA (verteporfin, dimension is for the pool fen).
(2) tried the green porphyrin class of benzo leaf each concentration of target compound and different incubation time back light the light power lethal effect of tumour cell is had bigger difference.The cell light power lethal effect that the 24h back light is hatched in administration is better than the cell light power lethal effect (table 3 and table 4) that the 4h back light is hatched in administration.
(3) as seen, at identical concentration (the 2.5 μ g.mL that tried by table 2 and table 4
-1) under, identical incubation time (24h) back is with same light dosage (10J.cm
-2) irradiation, it is suitable with BPDMA to the moving effectiveness of killing and wounding of the light of people's liver cancer BEL7402 cell to be tried the green porphyrin class of benzo leaf target compound, but the dark toxicity of The compounds of this invention pair cell is well below BPDMA, differ 100 times nearly, illustrate that the The compounds of this invention benzoporphyrin chlorophyll photosensitizer has efficiently, the characteristics (table 5) of low toxicity.
Table 5 administration is hatched and is tried target compound and BPDMA dark toxicity and the light power lethal effect to people's liver cancer BEL7402 cell behind the 24h
Annotate: reagent concentration is 2.5 μ g.mL
-1Illuminating dose is 10J.cm
-2
The green porphyrins of benzo leaf of the present invention has good light power lethal effect to people's liver cancer BEL7402 cell, and has advantage efficient, low toxicity.Therefore, The compounds of this invention can be used for preparing the medicine of photosensitive antitumor drug and the optimum vascular conditions of optical dynamic therapy such as senile macular degeneration SMD (a kind of retinal microvascular proliferative disease) and nevus flammeus (a kind of congenital skin capillary blood vessel deformity pathology).
Claims (4)
1. green porphyrins of benzo leaf, chemical structure of general formula be suc as formula shown in (I),
Wherein:
R
1Represent H, CH
3, CO
2CH
3, CH
2CO
2CH
3, CHCO
2CH
3
R
2Represent COOCH
3, CO, work as R
2During for CO and R
1Be CHCOOCH
3Form 5 yuan of rings;
R
3Represent H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
In the formula, work as R
1During for H, R
3Be (CH
2)
mOH, (CH
2)
mNR
4R
5
R
4And R
5Represent low alkyl group independently;
M represents the integer between the 2-6;
Described low alkyl group is meant the straight or branched alkyl that contains 1-6 carbon atom.
2. by the green porphyrins of the described benzo leaf of claim 1, it is characterized in that the R of described compound
1, R
2, R
3Be respectively:
3. claim 1 or the green porphyrins of the 2 described benzo leaves application in preparation light power curing cancer drug or optimum vascular conditions medicine of optical dynamic therapy or nevus flammeus medicine.
4. the preparation method of claim 1 or the green porphyrins of 2 described benzo leaves, synthetic route is as follows:
(1) is the feedstock production compound VI with the chlorophyll a, comprises chlorin f VI
1, chlorin p
6VI
2, chlorin e
6VI
3And chlorin e
4VI
4, reaction process is:
(2) prepare the green porphyrins I of target compound benzo leaf with compound VI, reaction process is:
Wherein:
When R is H, R '=R
1=H, R
2=CO
2CH
3, R
3=(CH
2)
mOH, (CH
2)
mNR
4R
5
When R is CO
2During H, R '=R
1=CO
2CH
3, R
2=CO
2CH
3, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
When R is CH
2CO
2During H, R '=CH
2CO
2CH
3, R
1=CH
2CO
2CH
3, CHCO
2CH
3, R
2=CO
2CH
3,-CO works as R
2During for CO and R
1Be CHCOOCH
3Form 5 yuan of rings, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
When R is CH
3The time, R '=R
1=CH
3, R
2=CO
2CH
3, R
3=H, low alkyl group, (CH
2)
mOH, (CH
2)
mNR
4R
5
R
4And R
5Represent low alkyl group independently;
M represents the integer between the 2-6; Described low alkyl group refers to contain the straight or branched alkyl of 1-6 carbon atom;
Concrete synthesis step is:
At first be the feedstock production pheophorbide acid a, prepare chlorin f VI respectively by pheophorbide acid a again with the chlorophyll a
1, chlorin p
6VI
2, chlorin e
6VI
3And chlorin e
4VI
4:
(1) preparation pheophorbide acid a
The diethyl ether solution of commercially available chlorophyll paste generates pheophorbide acid a through concentrated hydrochloric acid stirring reaction 2h under less than 10 ℃ cold condition;
(2) preparation chlorin f VI
1
Pheophorbide acid a and 25% potassium hydroxide ethanol liquid, logical O under 0 ℃ of condition
2Behind the reaction 1h, logical again N
2Back flow reaction 0.5h generates VI rapidly
1
(3) preparation chlorin p
6VI
2
Pheophorbide acid a ether solution and 25% potassium hydroxide n-propyl alcohol liquid, logical O under 0 ℃ of condition
2Reaction 2h generates C.I. Natural Red 8-18, and C.I. Natural Red 8-18 is in alkaline aqueous solution, and its hexa-atomic inner-acid anhydride ring splits voluntarily and quantitatively is transformed into VI
2
(4) preparation chlorin e
6VI
3With chlorin e
4VI
4
Pheophorbide acid a and 25% potassium hydroxide ethanol liquid are at logical N
2Following back flow reaction 1h generates VI
3Again with VI
3Back flow reaction 1h generates VI in pyridine
4
Again respectively by compound VI
1, VI
2, VI
3Or VI
4The green porphyrin class of preparation benzo leaf target Compound I:
(1) preparation chlorin f dimethyl ester V
1, chlorin p
6Trimethyl V
2, chlorin e
6Trimethyl V
3And chlorin e
4Dimethyl ester V
4:
Respectively with compound VI
1, VI
2, VI
3And VI
4The diazomethane CH of tetrahydrofuran THF liquid and 2.8% (w/v)
2N
2Ether solution reaction 10min promptly gets compound V
1, V
2, V
3Or V
4
(2) the green porphyrin f of preparation leaf dimethyl ester IV
1, the green porphyrin p of leaf
6Trimethyl IV
2, the green porphyrin e of leaf
6Trimethyl IV
3And the green porphyrin e of leaf
4Dimethyl ester IV
4:
Respectively with compound V
1, V
2, V
3And V
4Dichloromethane solution and 2,3-two chloro-5,6-dicyano-1,4-benzoquinones DDQ reaction promptly gets compound IV
1, IV
2, IV
3Or IV
4
(3) the green porphyrin f of preparation benzo leaf dimethyl ester III
1, the green porphyrin p of benzo leaf
6Trimethyl III
2, the green porphyrin e of benzo leaf
6Trimethyl III
3And the green porphyrin e of benzo leaf
4Dimethyl ester III
4:
Respectively with compound IV
1, IV
2, IV
3And IV
4With dimethyl butyn DMAD logical N in toluene liquid
2Refluxed 7 days, and carried out the Diels-Alder cycloaddition reaction, promptly get compound III
1, III
2, III
3Or III
4
(4) the green porphyrin f of preparation benzo leaf dimethyl ester TEA resets trans-isomer(ide) II
1, the green porphyrin p of benzo leaf
6Trimethyl TEA resets trans-isomer(ide) II
2, the green porphyrin e of benzo leaf
6Trimethyl TEA resets trans-isomer(ide) II
3And the green porphyrin e of benzo leaf
4Dimethyl ester TEA resets trans-isomer(ide) II
4: respectively with compound III
1, III
2, III
3And III
4Dichloromethane solution and triethylamine TEA reaction 4h, promptly get Compound I I
1, II
2, II
3Or II
4
(5) the green porphyrin f of preparation target compound benzo leaf dimethyl ester DBU resets cis-isomeride I
1, the green porphyrin p of benzo leaf
6Trimethyl DBU resets cis-isomeride I
2, the green porphyrin e of benzo leaf
6Trimethyl DBU resets cis-isomeride I
3, the green porphyrin e of benzo leaf
4Dimethyl ester DBU resets cis-isomeride I
4And the green porphyrin e of benzo leaf
6Trimethyl DBU resets and Dickman condensation cis-isomeride I
5:
Respectively with Compound I I
1, II
2And II
4Dichloromethane solution and DBU room temperature reaction 30min, promptly get target compound I
1, I
2Or I
4Compound I I
3Dichloromethane solution and DBU room temperature reaction 4h, promptly get target compound I
3And I
5
(6) the green porphyrin f of preparation target compound benzo leaf mono-methyl DBU resets cis-isomeride I
6, the green porphyrin p of benzo leaf
6Dimethyl ester DBU resets cis-isomeride I
7, the green porphyrin e of benzo leaf
6Dimethyl ester DBU resets cis-isomeride I
8, the green porphyrin e of benzo leaf
4Mono-methyl DBU resets cis-isomeride I
9And the green porphyrin e of benzo leaf
6Dimethyl ester DBU resets and Dickman condensation cis-isomeride I
10:
Respectively with Compound I
1, I
2, I
3, I
4And I
5Through the reaction of 25% hydrochloric acid directionally hydrolyzing, promptly get target compound I
6, I
7, I
8, I
9Or I
10
(7) the green porphyrin target compound of preparation benzo leaf I
11, I
12, I
13, I
14, I
15, I
16, I
17, I
18, I
19And I
20:
With Compound I
6Dichloromethane solution and corresponding substituted alcohols R
3OH reacts under dicyclohexylurea (DCU) DCC existence condition, promptly gets target compound I
11Or I
16
With Compound I
7Dichloromethane solution and corresponding substituted alcohols R
3OH reacts under dicyclohexylurea (DCU) DCC existence condition, promptly gets target compound I
12Or I
17
With Compound I
8Dichloromethane solution and corresponding substituted alcohols R
3OH reacts under dicyclohexylurea (DCU) DCC existence condition, promptly gets target compound I
13Or I
18
With Compound I
9Dichloromethane solution and corresponding substituted alcohols R
3OH reacts under dicyclohexylurea (DCU) DCC existence condition, promptly gets target compound I
14Or I
19
With Compound I
10Dichloromethane solution and corresponding substituted alcohols R
3OH reacts under dicyclohexylurea (DCU) DCC existence condition, promptly gets target compound I
15Or I
20
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
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| CN102503947A (en) * | 2011-11-02 | 2012-06-20 | 文剑 | Photosensitizer chlorin e6 titanium compound for treating tumors by photo-oxygen dynamic and preparation method thereof |
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| CN105384743A (en) * | 2015-11-12 | 2016-03-09 | 中国人民解放军第二军医大学 | Pyropheophorbide-a ether amino acid derivative as well as preparation method and application thereof |
| CN105601638B (en) * | 2016-01-28 | 2018-10-26 | 东北林业大学 | A kind of chlorophyllin derivative and preparation method thereof, as the application of photosensitive bacteriostatic agent and light sensitive pesticides |
| CN106046008A (en) * | 2016-05-25 | 2016-10-26 | 中国人民解放军第二军医大学 | Chlorin p6 amino acid derivative, preparation method therefor and use of chlorin p6 amino acid derivative |
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| 苯并卟啉衍生物对小鼠肉瘤180的光动力疗效. 余建鑫等.中国激光医学杂志，第8卷第2期. 1999 * |
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| CN102503947A (en) * | 2011-11-02 | 2012-06-20 | 文剑 | Photosensitizer chlorin e6 titanium compound for treating tumors by photo-oxygen dynamic and preparation method thereof |
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