IP Library Granted Patent US 11,939,332
Granted Patent B2
US 11,939,332 · App. 17/089,573 · Granted Mar 26, 2024

Synthesis of coelenterazine

Inventors: Rajagopala Reddy Duvvuru (Hyderabad, IN); Rama Bhatt (Newcastle, WA); Anil Kumar (Puyallup, WA)
Assignee: INTERNATIONAL PAPER COMPANY
C07D487/04B01J20/22B01J31/2404B01J2531/824C07B51/00
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Quick Facts
Patent No.
US 11,939,332
App. No.
17/089,573
Granted
Mar 26, 2024
Kind
B2
Abstract

Disclosed herein are synthesis methods for coelenterazine. Also disclosed are articles including the coelenterazine and coelenterazine derivatives. Representative absorbent articles include disposable diapers and adult incontinence products.

Claims (17)

1. A method of making coelenterazine, comprising:

(a) reacting 3-benzylpyrazin-2-amine (25) with N-bromosuccinimide to provide 3-benzyl-5-bromopyrazin-2-amine (2);

(b) reacting the 3-benzyl-5-bromopyrazin-2-amine (2) in two sequential steps to provide 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7) (coelenteramine); and

(c) coupling the 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7) with silyl-protected 1,1-diethoxy-3-(4-hydroxyphenyl)propan-2-one to provide coelenterazine, or a salt thereof.

2. The method of claim 1 , wherein (b) comprises a first step of reacting the 3-benzyl-5-bromopyrazin-2-amine (2) with 4-methoxyphenyl boronic acid (4) in the presence of a palladium catalyst to provide 3-benzyl-5-(4-methoxyphenyl)pyrazin-2-amine (5), and a second step of deprotecting the 3-benzyl-5-(4-methoxyphenyl)pyrazin-2-amine (5) to provide the 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7).

3. The method of claim 1 , wherein the silyl protected 1,1-diethoxy-3-(4-hydroxyphenyl)propan-2-one is 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1,1-diethoxypropan-2-one (23) and wherein the 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1,1-diethoxypropan-2-one (23) is synthesized by:

i. reacting 4-hydroxybenzaldehyde (8) with tert-butyldimethylsilyl chloride to provide 4-((tert-butyldimethylsilyl)oxy)benzaldehyde;

ii. reacting the 4-((tert-butyldimethylsilyl)oxy)benzaldehyde with sodium borohydride to provide (4-((tert-butyldimethylsilyl)oxy)phenyl)methanol;

iii. reacting the (4-((tert-butyldimethylsilyl)oxy)phenyl)methanol with methanesulfonyl chloride to provide tert-butyl(4-(chloromethyl)phenoxy)dimethylsilane (21);

iv. reacting the tert-butyl(4-(chloromethyl)phenoxy)dimethylsilane (21) with magnesium to provide (4-((tert-butyldimethylsilyl)oxy)benzyl)magnesium chloride; and

v. reacting the (4-((tert-butyldimethylsilyl)oxy)benzyl)magnesium chloride with ethyl 2,2-diethoxyacetate to provide the 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1,1-diethoxypropan-2-one (23).

4. The method of claim 3 , wherein 3-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1,1-diethoxypropan-2-one (23) is further purified by chromatography with an eluant comprising triethylamine.

5. A method of making an absorbent article, comprising incorporating the coelenterazine, or a salt thereof, made according to the method of claim 1 into an absorbent article.

6. An absorbent article, comprising the coelenterazine, or a salt thereof, synthesized by the method of claim 1 .

7. The method of claim 1 , wherein the coelenterazine, or salt thereof, is isolated in a composition; wherein the composition further comprises 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7).

8. The method of claim 7 , wherein when measured using liquid chromatography-mass spectrometry, the composition comprises a coelenterazine elution peak and a 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7) elution peak, and the integrated peak ratio of the coelenterazine elution peak to the 4-(5-amino-6-benzylpyrazin-2-yl)phenol (7) elution peak is 20:1 or more and/or 100:1 or less.

9. An absorbent article, comprising the composition made according to the method of claim 7 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2025
From: INTERNATIONAL PAPER COMPANY
To: GCF US HOLDINGS LLC
Reel/Frame 073563/0717 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2021
From: DUVVURU, RAJAGOPALA REDDY; KUMAR, ANIL; BHATT, RAMA
To: INTERNATIONAL PAPER COMPANY
Reel/Frame 055109/0498 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2020
From: DUVVURU, RAJAGOPALA REDDY; BHATT, RAMA; KUMAR, ANIL
To: INTERNATIONAL PAPER COMPANY
Reel/Frame 054328/0099 →